Canonical Allele Identifier: CA1627477799

Gene: RHAG

Linked Data

• dbSNP Id: rs1762702720

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49618917_49618924del , CM000668.2:g.49618917_49618924del	GRCh38
NC_000006.11:g.49586630_49586637del , CM000668.1:g.49586630_49586637del	GRCh37
NC_000006.10:g.49694589_49694596del	NCBI36
NG_011704.1:g.22953_22960del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.341+257_341+264del MANE Select	ENSP00000360217.4:n.341+257_341+264del
ENST00000642530.1:n.616+257_616+264del
ENST00000646272.1:c.341+257_341+264del	ENSP00000494337.1:n.341+257_341+264del
ENST00000646939.1:c.341+257_341+264del	ENSP00000494709.1:n.341+257_341+264del
ENST00000646963.1:c.341+257_341+264del	ENSP00000495337.1:n.341+257_341+264del
ENST00000229810.9:c.341+257_341+264del	ENSP00000229810.8:n.341+257_341+264del
ENST00000371175.8:c.341+257_341+264del	ENSP00000360217.4:n.341+257_341+264del
ENST00000618248.3:c.341+257_341+264del	ENSP00000482984.1:n.341+257_341+264del
NM_000324.2:c.341+257_341+264del	NP_000315.2:n.341+257_341+264del
XM_011514788.1:c.341+257_341+264del	XP_011513090.1:n.341+257_341+264del
NM_000324.3:c.341+257_341+264del MANE Select	NP_000315.2:n.341+257_341+264del