Canonical Allele Identifier: CA1515644832

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439639C= , CM000666.2:g.177439639C=	GRCh38
NC_000004.11:g.178360793C= , CM000666.1:g.178360793C=	GRCh37
NC_000004.10:g.178597787C=	NCBI36
NG_011845.2:g.7865G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.331G= MANE Select	ENSP00000264595.2:p.Ala111=
ENST00000264595.6:c.331G=	ENSP00000264595.2:p.Ala111=
ENST00000506853.5:n.365G=
ENST00000510635.1:c.27G=
ENST00000510955.5:n.315+634G=
NM_000027.3:c.331G=	NP_000018.2:p.Ala111=
NM_001171988.1:c.331G=	NP_001165459.1:p.Ala111=
NR_033655.1:n.459G=
XM_006714123.2:c.331G=	XP_006714186.1:p.Ala111=
XR_001741155.2:n.425G=
NM_000027.4:c.331G= MANE Select	NP_000018.2:p.Ala111=
NM_001171988.2:c.331G=	NP_001165459.1:p.Ala111=
NR_033655.2:n.393G=