ENST00000420660.5 AAMP
Information
- Transcript ID
- ENST00000420660.5
- Genome
- hg19
- Position
- chr2:219,128,885-219,134,463
- Strand
- -
- CDS length
- 1,248
- Amino acid length
- 416
- Gene symbol
- AAMP
- Gene type
- protein-coding
- Gene description
- angio associated migratory cell protein
- Gene Entrez Gene ID
- 14
Variants
Display target variant
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Exon
Exon number | Start | Stop |
---|---|---|
10 | 219,128,885 | 219,129,331 |
9 | 219,129,743 | 219,129,897 |
8 | 219,130,094 | 219,130,184 |
7 | 219,130,302 | 219,130,405 |
6 | 219,130,554 | 219,130,669 |
5 | 219,130,787 | 219,130,870 |
4 | 219,131,166 | 219,131,310 |
3 | 219,131,570 | 219,131,709 |
2 | 219,132,217 | 219,132,336 |
1 | 219,134,105 | 219,134,463 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
10 | CDS | 219,129,256 | 219,129,331 |
9 | CDS | 219,129,743 | 219,129,897 |
8 | CDS | 219,130,094 | 219,130,184 |
7 | CDS | 219,130,302 | 219,130,405 |
6 | CDS | 219,130,554 | 219,130,669 |
5 | CDS | 219,130,787 | 219,130,870 |
4 | CDS | 219,131,166 | 219,131,310 |
3 | CDS | 219,131,570 | 219,131,709 |
2 | CDS | 219,132,217 | 219,132,336 |
1 | CDS | 219,134,105 | 219,134,321 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr2 | 218,264,162 | 218,269,740 | Link |
CDS sequence
ATGCTTCTCTCCGTACCTCTTACCGCCTCCCGAGCCCCATCTTCTAACCCTCTCCCCAAAGCAGATGACCTGGCCCAGGAGATGGAAGATGTGGACTTTGAGGAAGAAGAGGAGGAAGAGGGCAACGAAGAGGGCTGGGTTCTAGAACCCCAGGAAGGGGTGGTCGGCAGCATGGAGGGCCCCGACGATAGCGAGGTCACCTTTGCATTGCACTCAGCATCTGTGTTTTGTGTGAGCCTGGACCCCAAGACCAATACCTTGGCAGTGACCGGGGGTGAAGATGACAAAGCCTTCGTATGGCGGCTCAGCGATGGGGAGCTGCTCTTTGAGTGTGCAGGCCATAAAGACTCTGTGACTTGTGCTGGTTTCAGCCATGACTCCACTCTAGTGGCCACAGGGGACATGAGTGGCCTCTTGAAAGTGTGGCAGGTGGACACTAAGGAGGAGGTCTGGTCCTTTGAAGCGGGAGACCTGGAGTGGATGGAGTGGCATCCTCGGGCACCTGTCCTGTTGGCGGGCACAGCTGACGGCAACACCTGGATGTGGAAAGTCCCGAATGGTGACTGCAAGACCTTCCAGGGTCCCAACTGCCCAGCCACCTGTGGCCGAGTCCTCCCTGATGGGAAGAGAGCTGTGGTAGGCTATGAAGATGGGACCATCAGGATTTGGGACCTGAAGCAGGGAAGCCCTATCCATGTACTGAAAGGGACTGAGGGTCACCAGGGCCCACTCACCTGTGTTGCTGCCAACCAGGATGGCAGCTTGATCCTAACTGGCTCTGTGGACTGCCAGGCCAAGCTGGTCAGTGCCACCACCGGCAAGGTGGTGGGTGTTTTTAGACCTGAGACTGTGGCCTCCCAGCCCAGCCTGGGAGAAGGGGAGGAGAGTGAGTCCAACTCGGTGGAGTCCTTGGGCTTCTGCAGTGTGATGCCCCTGGCAGCTGTTGGCTACCTGGATGGGACCTTGGCCATCTATGACCTGGCTACGCAGACTCTTAGGCATCAGTGTCAGCACCAGTCGGGCATCGTGCAGCTGCTGTGGGAGGCAGGCACTGCCGTGGTATATACCTGCAGCCTGGATGGCATCGTGCGCCTCTGGGACGCCCGGACCGGCCGCCTGCTTACTGACTACCGGGGCCACACGGCTGAGATCCTGGACTTTGCCCTCAGCAAAGATGCCTCCCTGGTGGTGACCACGTCAGGAGACCACAAAGCGAAAGTATTTTGTGTCCAAAGGCCTGACCGTTAA
Amino sequence
MLLSVPLTASRAPSSNPLPKADDLAQEMEDVDFEEEEEEEGNEEGWVLEPQEGVVGSMEGPDDSEVTFALHSASVFCVSLDPKTNTLAVTGGEDDKAFVWRLSDGELLFECAGHKDSVTCAGFSHDSTLVATGDMSGLLKVWQVDTKEEVWSFEAGDLEWMEWHPRAPVLLAGTADGNTWMWKVPNGDCKTFQGPNCPATCGRVLPDGKRAVVGYEDGTIRIWDLKQGSPIHVLKGTEGHQGPLTCVAANQDGSLILTGSVDCQAKLVSATTGKVVGVFRPETVASQPSLGEGEESESNSVESLGFCSVMPLAAVGYLDGTLAIYDLATQTLRHQCQHQSGIVQLLWEAGTAVVYTCSLDGIVRLWDARTGRLLTDYRGHTAEILDFALSKDASLVVTTSGDHKAKVFCVQRPDR*