Canonical Allele Identifier: CA122826
Gene: RHAG HGNC NCBI

Linked Data

ClinVar Variation Id: 13057
ClinVar RCV Id: RCV000013932
dbSNP Id: rs387906519
MyVariant Identifiers: chr6:g.49604369_49604372delinsTC (hg19) chr6:g.49636656_49636659delinsTC (hg38)
PubMed: PMID:8563755
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49636656_49636659delinsTC , CM000668.2:g.49636656_49636659delinsTC GRCh38
NC_000006.11:g.49604369_49604372delinsTC , CM000668.1:g.49604369_49604372delinsTC GRCh37
NC_000006.10:g.49712328_49712331delinsTC NCBI36
NG_011704.1:g.5216_5219delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000371175.10:c.154_157delinsGA MANE Select ENSP00000360217.4:p.Pro52AspfsTer?
ENST00000642530.1:n.181_184delinsGA
ENST00000646272.1:c.154_157delinsGA ENSP00000494337.1:p.Pro52AspfsTer?
ENST00000646939.1:c.154_157delinsGA ENSP00000494709.1:p.Pro52AspfsTer?
ENST00000646963.1:c.154_157delinsGA ENSP00000495337.1:p.Pro52AspfsTer?
ENST00000229810.9:c.154_157delinsGA ENSP00000229810.8:p.Pro52AspfsTer?
ENST00000371175.8:c.154_157delinsGA ENSP00000360217.4:p.Pro52AspfsTer?
ENST00000618248.3:c.154_157delinsGA ENSP00000482984.1:p.Pro52AspfsTer?
NM_000324.2:c.154_157delinsGA NP_000315.2:p.Pro52AspfsTer?
XM_011514788.1:c.154_157delinsGA XP_011513090.1:p.Pro52AspfsTer?
NM_000324.3:c.154_157delinsGA MANE Select NP_000315.2:p.Pro52AspfsTer?
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