GYPA glycophorin A (MNS blood group)
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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22 |
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2 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | CD235a |
SYNONYM | GPA |
SYNONYM | GPErik |
SYNONYM | GPSAT |
SYNONYM | HGpMiV |
SYNONYM | HGpMiXI |
SYNONYM | HGpSta(C) |
SYNONYM | MN |
SYNONYM | MNS |
SYNONYM | PAS-2 |
MIM | 617922 OMIM |
HGNC | HGNC:4702 HGNC |
Ensembl | ENSG00000170180 Ensembl |
AllianceGenome | HGNC:4702 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000512789.5 | hg38 | chr4 | 144,111,394 | 144,140,635 | 29,242 |
ENST00000512064.5 | hg38 | chr4 | 144,111,367 | 144,140,635 | 29,269 |
ENST00000642713.1 | hg38 | chr4 | 144,111,355 | 144,140,661 | 29,307 |
ENST00000641688.3 | hg38 | chr4 | 144,109,303 | 144,140,718 | 31,416 |
ENST00000324022.14 | hg38 | chr4 | 144,111,055 | 144,140,693 | 29,639 |
ENST00000616983.4 | hg38 | chr4 | 144,109,303 | 144,127,908 | 18,606 |
ENST00000642295.1 | hg38 | chr4 | 144,110,851 | 144,140,674 | 29,824 |
ENST00000360771.8 | hg38 | chr4 | 144,109,304 | 144,140,751 | 31,448 |
ENST00000503627.2 | hg38 | chr4 | 144,111,394 | 144,140,635 | 29,242 |
ENST00000643148.1 | hg38 | chr4 | 144,111,350 | 144,140,672 | 29,323 |
ENST00000504786.5 | hg38 | chr4 | 144,111,394 | 144,140,635 | 29,242 |
ENST00000535709.6 | hg38 | chr4 | 144,111,344 | 144,140,674 | 29,331 |
ENST00000646447.1 | hg38 | chr4 | 144,111,344 | 144,140,674 | 29,331 |
ENST00000616983.4 | hg19 | chr4 | 145,030,456 | 145,049,061 | 18,606 |
ENST00000641688.3 | hg19 | chr4 | 145,030,456 | 145,061,871 | 31,416 |
ENST00000360771.8 | hg19 | chr4 | 145,030,457 | 145,061,904 | 31,448 |
ENST00000642295.1 | hg19 | chr4 | 145,032,004 | 145,061,827 | 29,824 |
ENST00000324022.14 | hg19 | chr4 | 145,032,208 | 145,061,846 | 29,639 |
ENST00000535709.6 | hg19 | chr4 | 145,032,497 | 145,061,827 | 29,331 |
ENST00000643148.1 | hg19 | chr4 | 145,032,503 | 145,061,825 | 29,323 |
ENST00000512789.5 | hg19 | chr4 | 145,032,547 | 145,061,788 | 29,242 |
ENST00000504786.5 | hg19 | chr4 | 145,032,547 | 145,061,788 | 29,242 |
ENST00000503627.2 | hg19 | chr4 | 145,032,547 | 145,061,788 | 29,242 |
ENST00000512064.5 | hg19 | chr4 | 145,032,520 | 145,061,788 | 29,269 |
ENST00000642713.1 | hg19 | chr4 | 145,032,508 | 145,061,814 | 29,307 |
ENST00000646447.1 | hg19 | chr4 | 145,032,497 | 145,061,827 | 29,331 |
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