Canonical Allele Identifier: CA1515645135

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439783T= , CM000666.2:g.177439783T=	GRCh38
NC_000004.11:g.178360937T= , CM000666.1:g.178360937T=	GRCh37
NC_000004.10:g.178597931T=	NCBI36
NG_011845.2:g.7721A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.282-95A= MANE Select	ENSP00000264595.2:n.282-95A=
ENST00000264595.6:c.282-95A=	ENSP00000264595.2:n.282-95A=
ENST00000506853.5:n.316-95A=
ENST00000510955.5:n.315+490A=
NM_000027.3:c.282-95A=	NP_000018.2:n.282-95A=
NM_001171988.1:c.282-95A=	NP_001165459.1:n.282-95A=
NR_033655.1:n.410-95A=
XM_006714123.2:c.282-95A=	XP_006714186.1:n.282-95A=
XR_001741155.2:n.376-95A=
NM_000027.4:c.282-95A= MANE Select	NP_000018.2:n.282-95A=
NM_001171988.2:c.282-95A=	NP_001165459.1:n.282-95A=
NR_033655.2:n.344-95A=