Canonical Allele Identifier: CA1515643513

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438788T= , CM000666.2:g.177438788T=	GRCh38
NC_000004.11:g.178359942T= , CM000666.1:g.178359942T=	GRCh37
NC_000004.10:g.178596936T=	NCBI36
NG_011845.2:g.8716A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.464A= MANE Select	ENSP00000264595.2:p.His155=
ENST00000264595.6:c.464A=	ENSP00000264595.2:p.His155=
ENST00000502310.5:c.119A=	ENSP00000423798.1:p.His40=
ENST00000506853.5:n.498A=
ENST00000510635.1:c.160A=
ENST00000510955.5:n.385A=
NM_000027.3:c.464A=	NP_000018.2:p.His155=
NM_001171988.1:c.464A=	NP_001165459.1:p.His155=
NR_033655.1:n.592A=
XM_006714123.2:c.464A=	XP_006714186.1:p.His155=
XR_001741155.2:n.558A=
NM_000027.4:c.464A= MANE Select	NP_000018.2:p.His155=
NM_001171988.2:c.464A=	NP_001165459.1:p.His155=
NR_033655.2:n.526A=