Canonical Allele Identifier: CA1515643313

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438669C= , CM000666.2:g.177438669C=	GRCh38
NC_000004.11:g.178359823C= , CM000666.1:g.178359823C=	GRCh37
NC_000004.10:g.178596817C=	NCBI36
NG_011845.2:g.8835G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.507+76G= MANE Select	ENSP00000264595.2:n.507+76G=
ENST00000264595.6:c.507+76G=	ENSP00000264595.2:n.507+76G=
ENST00000502310.5:c.162+76G=	ENSP00000423798.1:n.162+76G=
ENST00000506853.5:n.541+76G=
ENST00000510635.1:c.203+76G=
ENST00000510955.5:n.428+76G=
NM_000027.3:c.507+76G=	NP_000018.2:n.507+76G=
NM_001171988.1:c.507+76G=	NP_001165459.1:n.507+76G=
NR_033655.1:n.635+76G=
XM_006714123.2:c.507+76G=	XP_006714186.1:n.507+76G=
XR_001741155.2:n.601+76G=
NM_000027.4:c.507+76G= MANE Select	NP_000018.2:n.507+76G=
NM_001171988.2:c.507+76G=	NP_001165459.1:n.507+76G=
NR_033655.2:n.569+76G=