Canonical Allele Identifier: CA1515637752

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177434478T= , CM000666.2:g.177434478T=	GRCh38
NC_000004.11:g.178355632T= , CM000666.1:g.178355632T=	GRCh37
NC_000004.10:g.178592626T=	NCBI36
NG_011845.2:g.13026A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.710A= MANE Select	ENSP00000264595.2:p.Asp237=
ENST00000264595.6:c.710A=	ENSP00000264595.2:p.Asp237=
ENST00000502310.5:c.281A=	ENSP00000423798.1:p.Asp94=
ENST00000506853.5:n.668A=
ENST00000510635.1:c.376A=
NM_000027.3:c.710A=	NP_000018.2:p.Asp237=
NM_001171988.1:c.680A=	NP_001165459.1:p.Asp227=
NR_033655.1:n.762A=
XM_006714123.2:c.*4A=	XP_006714186.1:n.*4A=
XR_001741155.2:n.782A=
NM_000027.4:c.710A= MANE Select	NP_000018.2:p.Asp237=
NM_001171988.2:c.680A=	NP_001165459.1:p.Asp227=
NR_033655.2:n.696A=