Canonical Allele Identifier: CA1515645059

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439722G= , CM000666.2:g.177439722G=	GRCh38
NC_000004.11:g.178360876G= , CM000666.1:g.178360876G=	GRCh37
NC_000004.10:g.178597870G=	NCBI36
NG_011845.2:g.7782C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.282-34C= MANE Select	ENSP00000264595.2:n.282-34C=
ENST00000264595.6:c.282-34C=	ENSP00000264595.2:n.282-34C=
ENST00000506853.5:n.316-34C=
ENST00000510955.5:n.315+551C=
NM_000027.3:c.282-34C=	NP_000018.2:n.282-34C=
NM_001171988.1:c.282-34C=	NP_001165459.1:n.282-34C=
NR_033655.1:n.410-34C=
XM_006714123.2:c.282-34C=	XP_006714186.1:n.282-34C=
XR_001741155.2:n.376-34C=
NM_000027.4:c.282-34C= MANE Select	NP_000018.2:n.282-34C=
NM_001171988.2:c.282-34C=	NP_001165459.1:n.282-34C=
NR_033655.2:n.344-34C=