Canonical Allele Identifier: CA1515644640

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439583T= , CM000666.2:g.177439583T=	GRCh38
NC_000004.11:g.178360737T= , CM000666.1:g.178360737T=	GRCh37
NC_000004.10:g.178597731T=	NCBI36
NG_011845.2:g.7921A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.387A= MANE Select	ENSP00000264595.2:p.Gly129=
ENST00000264595.6:c.387A=	ENSP00000264595.2:p.Gly129=
ENST00000502310.5:c.42A=	ENSP00000423798.1:p.Gly14=
ENST00000506853.5:n.421A=
ENST00000510635.1:c.83A=
ENST00000510955.5:n.315+690A=
NM_000027.3:c.387A=	NP_000018.2:p.Gly129=
NM_001171988.1:c.387A=	NP_001165459.1:p.Gly129=
NR_033655.1:n.515A=
XM_006714123.2:c.387A=	XP_006714186.1:p.Gly129=
XR_001741155.2:n.481A=
NM_000027.4:c.387A= MANE Select	NP_000018.2:p.Gly129=
NM_001171988.2:c.387A=	NP_001165459.1:p.Gly129=
NR_033655.2:n.449A=