Canonical Allele Identifier: CA1627478020
Gene: RHAG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49619366_49619367delinsGA , CM000668.2:g.49619366_49619367delinsGA GRCh38
NC_000006.11:g.49587079_49587080delinsGA , CM000668.1:g.49587079_49587080delinsGA GRCh37
NC_000006.10:g.49695038_49695039delinsGA NCBI36
NG_011704.1:g.22508_22509delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371175.10:c.158-5_158-4delinsTC MANE Select ENSP00000360217.4:n.158-5_158-4delinsTC
ENST00000642530.1:n.433-5_433-4delinsTC
ENST00000646272.1:c.158-5_158-4delinsTC ENSP00000494337.1:n.158-5_158-4delinsTC
ENST00000646939.1:c.158-5_158-4delinsTC ENSP00000494709.1:n.158-5_158-4delinsTC
ENST00000646963.1:c.158-5_158-4delinsTC ENSP00000495337.1:n.158-5_158-4delinsTC
ENST00000229810.9:c.158-5_158-4delinsTC ENSP00000229810.8:n.158-5_158-4delinsTC
ENST00000371175.8:c.158-5_158-4delinsTC ENSP00000360217.4:n.158-5_158-4delinsTC
ENST00000618248.3:c.158-5_158-4delinsTC ENSP00000482984.1:n.158-5_158-4delinsTC
NM_000324.2:c.158-5_158-4delinsTC NP_000315.2:n.158-5_158-4delinsTC
XM_011514788.1:c.158-5_158-4delinsTC XP_011513090.1:n.158-5_158-4delinsTC
NM_000324.3:c.158-5_158-4delinsTC MANE Select NP_000315.2:n.158-5_158-4delinsTC