Canonical Allele Identifier: CA2679058351

Gene: RHAG

Linked Data

• gnomAD v4: 6-49619318-G-GGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619320_49619322dup , CM000668.2:g.49619320_49619322dup	GRCh38
NC_000006.11:g.49587033_49587035dup , CM000668.1:g.49587033_49587035dup	GRCh37
NC_000006.10:g.49694992_49694994dup	NCBI36
NG_011704.1:g.22554_22556dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.199_201dup MANE Select	ENSP00000360217.4:p.Phe67_Leu68insPhe
ENST00000642530.1:n.474_476dup
ENST00000646272.1:c.199_201dup	ENSP00000494337.1:p.Phe67_Leu68insPhe
ENST00000646939.1:c.199_201dup	ENSP00000494709.1:p.Phe67_Leu68insPhe
ENST00000646963.1:c.199_201dup	ENSP00000495337.1:p.Phe67_Leu68insPhe
ENST00000229810.9:c.199_201dup	ENSP00000229810.8:p.Phe67_Leu68insPhe
ENST00000371175.8:c.199_201dup	ENSP00000360217.4:p.Phe67_Leu68insPhe
ENST00000618248.3:c.199_201dup	ENSP00000482984.1:p.Phe67_Leu68insPhe
NM_000324.2:c.199_201dup	NP_000315.2:p.Phe67_Leu68insPhe
XM_011514788.1:c.199_201dup	XP_011513090.1:p.Phe67_Leu68insPhe
NM_000324.3:c.199_201dup MANE Select	NP_000315.2:p.Phe67_Leu68insPhe