Canonical Allele Identifier: CA1515643281

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438620C= , CM000666.2:g.177438620C=	GRCh38
NC_000004.11:g.178359774C= , CM000666.1:g.178359774C=	GRCh37
NC_000004.10:g.178596768C=	NCBI36
NG_011845.2:g.8884G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.507+125G= MANE Select	ENSP00000264595.2:n.507+125G=
ENST00000264595.6:c.507+125G=	ENSP00000264595.2:n.507+125G=
ENST00000502310.5:c.162+125G=	ENSP00000423798.1:n.162+125G=
ENST00000506853.5:n.541+125G=
ENST00000510635.1:c.203+125G=
ENST00000510955.5:n.428+125G=
NM_000027.3:c.507+125G=	NP_000018.2:n.507+125G=
NM_001171988.1:c.507+125G=	NP_001165459.1:n.507+125G=
NR_033655.1:n.635+125G=
XM_006714123.2:c.507+125G=	XP_006714186.1:n.507+125G=
XR_001741155.2:n.601+125G=
NM_000027.4:c.507+125G= MANE Select	NP_000018.2:n.507+125G=
NM_001171988.2:c.507+125G=	NP_001165459.1:n.507+125G=
NR_033655.2:n.569+125G=