Canonical Allele Identifier: CA2578699192

Gene: RHAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619211del , CM000668.2:g.49619211del	GRCh38
NC_000006.11:g.49586924del , CM000668.1:g.49586924del	GRCh37
NC_000006.10:g.49694883del	NCBI36
NG_011704.1:g.22665del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.310del MANE Select	ENSP00000360217.4:p.Gln104ArgfsTer12
ENST00000642530.1:n.585del
ENST00000646272.1:c.310del	ENSP00000494337.1:p.Gln104ArgfsTer12
ENST00000646939.1:c.310del	ENSP00000494709.1:p.Gln104ArgfsTer12
ENST00000646963.1:c.310del	ENSP00000495337.1:p.Gln104ArgfsTer12
ENST00000229810.9:c.310del	ENSP00000229810.8:p.Gln104ArgfsTer12
ENST00000371175.8:c.310del	ENSP00000360217.4:p.Gln104ArgfsTer12
ENST00000618248.3:c.310del	ENSP00000482984.1:p.Gln104ArgfsTer12
NM_000324.2:c.310del	NP_000315.2:p.Gln104ArgfsTer12
XM_011514788.1:c.310del	XP_011513090.1:p.Gln104ArgfsTer12
NM_000324.3:c.310del MANE Select	NP_000315.2:p.Gln104ArgfsTer12