Canonical Allele Identifier: CA1088827510

Gene: RHAG

Linked Data

• dbSNP Id: rs1762706053
• gnomAD v3: 6-49619047-TAA-T
• gnomAD v4: 6-49619047-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619049_49619050del , CM000668.2:g.49619049_49619050del	GRCh38
NC_000006.11:g.49586762_49586763del , CM000668.1:g.49586762_49586763del	GRCh37
NC_000006.10:g.49694721_49694722del	NCBI36
NG_011704.1:g.22826_22827del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.341+130_341+131del MANE Select	ENSP00000360217.4:n.341+130_341+131del
ENST00000642530.1:n.616+130_616+131del
ENST00000646272.1:c.341+130_341+131del	ENSP00000494337.1:n.341+130_341+131del
ENST00000646939.1:c.341+130_341+131del	ENSP00000494709.1:n.341+130_341+131del
ENST00000646963.1:c.341+130_341+131del	ENSP00000495337.1:n.341+130_341+131del
ENST00000229810.9:c.341+130_341+131del	ENSP00000229810.8:n.341+130_341+131del
ENST00000371175.8:c.341+130_341+131del	ENSP00000360217.4:n.341+130_341+131del
ENST00000618248.3:c.341+130_341+131del	ENSP00000482984.1:n.341+130_341+131del
NM_000324.2:c.341+130_341+131del	NP_000315.2:n.341+130_341+131del
XM_011514788.1:c.341+130_341+131del	XP_011513090.1:n.341+130_341+131del
NM_000324.3:c.341+130_341+131del MANE Select	NP_000315.2:n.341+130_341+131del