Canonical Allele Identifier: CA1515645149

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439806G= , CM000666.2:g.177439806G=	GRCh38
NC_000004.11:g.178360960G= , CM000666.1:g.178360960G=	GRCh37
NC_000004.10:g.178597954G=	NCBI36
NG_011845.2:g.7698C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.282-118C= MANE Select	ENSP00000264595.2:n.282-118C=
ENST00000264595.6:c.282-118C=	ENSP00000264595.2:n.282-118C=
ENST00000506853.5:n.316-118C=
ENST00000510955.5:n.315+467C=
NM_000027.3:c.282-118C=	NP_000018.2:n.282-118C=
NM_001171988.1:c.282-118C=	NP_001165459.1:n.282-118C=
NR_033655.1:n.410-118C=
XM_006714123.2:c.282-118C=	XP_006714186.1:n.282-118C=
XR_001741155.2:n.376-118C=
NM_000027.4:c.282-118C= MANE Select	NP_000018.2:n.282-118C=
NM_001171988.2:c.282-118C=	NP_001165459.1:n.282-118C=
NR_033655.2:n.344-118C=