Canonical Allele Identifier: CA1339336166

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240878788G= , CM000664.2:g.240878788G=	GRCh38
NC_000002.11:g.241818205G= , CM000664.1:g.241818205G=	GRCh37
NC_000002.10:g.241466878G=	NCBI36
NG_008005.1:g.15044G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.1146G= MANE Select	ENSP00000302620.3:p.Ala382=
ENST00000307503.3:c.1146G=	ENSP00000302620.3:p.Ala382=
ENST00000470255.1:n.924G=
NM_000030.2:c.1146G=	NP_000021.1:p.Ala382=
NM_000030.3:c.1146G= MANE Select	NP_000021.1:p.Ala382=