Canonical Allele Identifier: CA1515643464

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438770C= , CM000666.2:g.177438770C=	GRCh38
NC_000004.11:g.178359924C= , CM000666.1:g.178359924C=	GRCh37
NC_000004.10:g.178596918C=	NCBI36
NG_011845.2:g.8734G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.482G= MANE Select	ENSP00000264595.2:p.Arg161=
ENST00000264595.6:c.482G=	ENSP00000264595.2:p.Arg161=
ENST00000502310.5:c.137G=	ENSP00000423798.1:p.Arg46=
ENST00000506853.5:n.516G=
ENST00000510635.1:c.178G=
ENST00000510955.5:n.403G=
NM_000027.3:c.482G=	NP_000018.2:p.Arg161=
NM_001171988.1:c.482G=	NP_001165459.1:p.Arg161=
NR_033655.1:n.610G=
XM_006714123.2:c.482G=	XP_006714186.1:p.Arg161=
XR_001741155.2:n.576G=
NM_000027.4:c.482G= MANE Select	NP_000018.2:p.Arg161=
NM_001171988.2:c.482G=	NP_001165459.1:p.Arg161=
NR_033655.2:n.544G=