Canonical Allele Identifier: CA1339333572

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240874012C= , CM000664.2:g.240874012C=	GRCh38
NC_000002.11:g.241813429C= , CM000664.1:g.241813429C=	GRCh37
NC_000002.10:g.241462102C=	NCBI36
NG_008005.1:g.10268C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000307503.4:c.630C= MANE Select	ENSP00000302620.3:p.Ala210=
ENST00000307503.3:c.630C=	ENSP00000302620.3:p.Ala210=
ENST00000476698.1:n.332+963C=
NM_000030.2:c.630C=	NP_000021.1:p.Ala210=
NM_000030.3:c.630C= MANE Select	NP_000021.1:p.Ala210=