Canonical Allele Identifier: CA1515645080

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439741G= , CM000666.2:g.177439741G=	GRCh38
NC_000004.11:g.178360895G= , CM000666.1:g.178360895G=	GRCh37
NC_000004.10:g.178597889G=	NCBI36
NG_011845.2:g.7763C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.282-53C= MANE Select	ENSP00000264595.2:n.282-53C=
ENST00000264595.6:c.282-53C=	ENSP00000264595.2:n.282-53C=
ENST00000506853.5:n.316-53C=
ENST00000510955.5:n.315+532C=
NM_000027.3:c.282-53C=	NP_000018.2:n.282-53C=
NM_001171988.1:c.282-53C=	NP_001165459.1:n.282-53C=
NR_033655.1:n.410-53C=
XM_006714123.2:c.282-53C=	XP_006714186.1:n.282-53C=
XR_001741155.2:n.376-53C=
NM_000027.4:c.282-53C= MANE Select	NP_000018.2:n.282-53C=
NM_001171988.2:c.282-53C=	NP_001165459.1:n.282-53C=
NR_033655.2:n.344-53C=