Canonical Allele Identifier: CA1339334186

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240875151C= , CM000664.2:g.240875151C=	GRCh38
NC_000002.11:g.241814568C= , CM000664.1:g.241814568C=	GRCh37
NC_000002.10:g.241463241C=	NCBI36
NG_008005.1:g.11407C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000307503.4:c.723C= MANE Select	ENSP00000302620.3:p.Tyr241=
ENST00000307503.3:c.723C=	ENSP00000302620.3:p.Tyr241=
ENST00000476698.1:n.375C=
NM_000030.2:c.723C=	NP_000021.1:p.Tyr241=
NM_000030.3:c.723C= MANE Select	NP_000021.1:p.Tyr241=