Canonical Allele Identifier: CA1515644917

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439662C= , CM000666.2:g.177439662C=	GRCh38
NC_000004.11:g.178360816C= , CM000666.1:g.178360816C=	GRCh37
NC_000004.10:g.178597810C=	NCBI36
NG_011845.2:g.7842G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.308G= MANE Select	ENSP00000264595.2:p.Gly103=
ENST00000264595.6:c.308G=	ENSP00000264595.2:p.Gly103=
ENST00000506853.5:n.342G=
ENST00000510635.1:c.4G=
ENST00000510955.5:n.315+611G=
NM_000027.3:c.308G=	NP_000018.2:p.Gly103=
NM_001171988.1:c.308G=	NP_001165459.1:p.Gly103=
NR_033655.1:n.436G=
XM_006714123.2:c.308G=	XP_006714186.1:p.Gly103=
XR_001741155.2:n.402G=
NM_000027.4:c.308G= MANE Select	NP_000018.2:p.Gly103=
NM_001171988.2:c.308G=	NP_001165459.1:p.Gly103=
NR_033655.2:n.370G=