Canonical Allele Identifier: CA2596907483

Gene: RHAG

Linked Data

• gnomAD v3: 6-49619057-GCCTTC-G
• gnomAD v4: 6-49619057-GCCTTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619058_49619062del , CM000668.2:g.49619058_49619062del	GRCh38
NC_000006.11:g.49586771_49586775del , CM000668.1:g.49586771_49586775del	GRCh37
NC_000006.10:g.49694730_49694734del	NCBI36
NG_011704.1:g.22813_22817del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.341+117_341+121del MANE Select	ENSP00000360217.4:n.341+117_341+121del
ENST00000642530.1:n.616+117_616+121del
ENST00000646272.1:c.341+117_341+121del	ENSP00000494337.1:n.341+117_341+121del
ENST00000646939.1:c.341+117_341+121del	ENSP00000494709.1:n.341+117_341+121del
ENST00000646963.1:c.341+117_341+121del	ENSP00000495337.1:n.341+117_341+121del
ENST00000229810.9:c.341+117_341+121del	ENSP00000229810.8:n.341+117_341+121del
ENST00000371175.8:c.341+117_341+121del	ENSP00000360217.4:n.341+117_341+121del
ENST00000618248.3:c.341+117_341+121del	ENSP00000482984.1:n.341+117_341+121del
NM_000324.2:c.341+117_341+121del	NP_000315.2:n.341+117_341+121del
XM_011514788.1:c.341+117_341+121del	XP_011513090.1:n.341+117_341+121del
NM_000324.3:c.341+117_341+121del MANE Select	NP_000315.2:n.341+117_341+121del