ENST00000420660.5 AAMP
Information
- Transcript ID
- ENST00000420660.5
- Genome
- hg38
- Position
- chr2:218,264,162-218,269,740
- 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
|
Category | : |
|
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 | 218,264,162 | 218,264,608 |
9 | 218,265,020 | 218,265,174 |
8 | 218,265,371 | 218,265,461 |
7 | 218,265,579 | 218,265,682 |
6 | 218,265,831 | 218,265,946 |
5 | 218,266,064 | 218,266,147 |
4 | 218,266,443 | 218,266,587 |
3 | 218,266,847 | 218,266,986 |
2 | 218,267,494 | 218,267,613 |
1 | 218,269,382 | 218,269,740 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
10 | CDS | 218,264,533 | 218,264,608 |
9 | CDS | 218,265,020 | 218,265,174 |
8 | CDS | 218,265,371 | 218,265,461 |
7 | CDS | 218,265,579 | 218,265,682 |
6 | CDS | 218,265,831 | 218,265,946 |
5 | CDS | 218,266,064 | 218,266,147 |
4 | CDS | 218,266,443 | 218,266,587 |
3 | CDS | 218,266,847 | 218,266,986 |
2 | CDS | 218,267,494 | 218,267,613 |
1 | CDS | 218,269,382 | 218,269,598 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr2 | 219,128,885 | 219,134,463 | Link |
CDS sequence
ATGCTTCTCTCCGTACCTCTTACCGCCTCCCGAGCCCCATCTTCTAACCCTCTCCCCAAAGCAGATGACCTGGCCCAGGAGATGGAAGATGTGGACTTTGAGGAAGAAGAGGAGGAAGAGGGCAACGAAGAGGGCTGGGTTCTAGAACCCCAGGAAGGGGTGGTCGGCAGCATGGAGGGCCCCGACGATAGCGAGGTCACCTTTGCATTGCACTCAGCATCTGTGTTTTGTGTGAGCCTGGACCCCAAGACCAATACCTTGGCAGTGACCGGGGGTGAAGATGACAAAGCCTTCGTATGGCGGCTCAGCGATGGGGAGCTGCTCTTTGAGTGTGCAGGCCATAAAGACTCTGTGACTTGTGCTGGTTTCAGCCATGACTCCACTCTAGTGGCCACAGGGGACATGAGTGGCCTCTTGAAAGTGTGGCAGGTGGACACTAAGGAGGAGGTCTGGTCCTTTGAAGCGGGAGACCTGGAGTGGATGGAGTGGCATCCTCGGGCACCTGTCCTGTTGGCGGGCACAGCTGACGGCAACACCTGGATGTGGAAAGTCCCGAATGGTGACTGCAAGACCTTCCAGGGTCCCAACTGCCCAGCCACCTGTGGCCGAGTCCTCCCTGATGGGAAGAGAGCTGTGGTAGGCTATGAAGATGGGACCATCAGGATTTGGGACCTGAAGCAGGGAAGCCCTATCCATGTACTGAAAGGGACTGAGGGTCACCAGGGCCCACTCACCTGTGTTGCTGCCAACCAGGATGGCAGCTTGATCCTAACTGGCTCTGTGGACTGCCAGGCCAAGCTGGTCAGTGCCACCACCGGCAAGGTGGTGGGTGTTTTTAGACCTGAGACTGTGGCCTCCCAGCCCAGCCTGGGAGAAGGGGAGGAGAGTGAGTCCAACTCGGTGGAGTCCTTGGGCTTCTGCAGTGTGATGCCCCTGGCAGCTGTTGGCTACCTGGATGGGACCTTGGCCATCTATGACCTGGCTACGCAGACTCTTAGGCATCAGTGTCAGCACCAGTCGGGCATCGTGCAGCTGCTGTGGGAGGCAGGCACTGCCGTGGTATATACCTGCAGCCTGGATGGCATCGTGCGCCTCTGGGACGCCCGGACCGGCCGCCTGCTTACTGACTACCGGGGCCACACGGCTGAGATCCTGGACTTTGCCCTCAGCAAAGATGCCTCCCTGGTGGTGACCACGTCAGGAGACCACAAAGCGAAAGTATTTTGTGTCCAAAGGCCTGACCGTTAA
Amino sequence
MLLSVPLTASRAPSSNPLPKADDLAQEMEDVDFEEEEEEEGNEEGWVLEPQEGVVGSMEGPDDSEVTFALHSASVFCVSLDPKTNTLAVTGGEDDKAFVWRLSDGELLFECAGHKDSVTCAGFSHDSTLVATGDMSGLLKVWQVDTKEEVWSFEAGDLEWMEWHPRAPVLLAGTADGNTWMWKVPNGDCKTFQGPNCPATCGRVLPDGKRAVVGYEDGTIRIWDLKQGSPIHVLKGTEGHQGPLTCVAANQDGSLILTGSVDCQAKLVSATTGKVVGVFRPETVASQPSLGEGEESESNSVESLGFCSVMPLAAVGYLDGTLAIYDLATQTLRHQCQHQSGIVQLLWEAGTAVVYTCSLDGIVRLWDARTGRLLTDYRGHTAEILDFALSKDASLVVTTSGDHKAKVFCVQRPDR*