Canonical Allele Identifier: CA1515645076

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439739T= , CM000666.2:g.177439739T=	GRCh38
NC_000004.11:g.178360893T= , CM000666.1:g.178360893T=	GRCh37
NC_000004.10:g.178597887T=	NCBI36
NG_011845.2:g.7765A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.282-51A= MANE Select	ENSP00000264595.2:n.282-51A=
ENST00000264595.6:c.282-51A=	ENSP00000264595.2:n.282-51A=
ENST00000506853.5:n.316-51A=
ENST00000510955.5:n.315+534A=
NM_000027.3:c.282-51A=	NP_000018.2:n.282-51A=
NM_001171988.1:c.282-51A=	NP_001165459.1:n.282-51A=
NR_033655.1:n.410-51A=
XM_006714123.2:c.282-51A=	XP_006714186.1:n.282-51A=
XR_001741155.2:n.376-51A=
NM_000027.4:c.282-51A= MANE Select	NP_000018.2:n.282-51A=
NM_001171988.2:c.282-51A=	NP_001165459.1:n.282-51A=
NR_033655.2:n.344-51A=