Canonical Allele Identifier: CA1339334182

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240875140T= , CM000664.2:g.240875140T=	GRCh38
NC_000002.11:g.241814557T= , CM000664.1:g.241814557T=	GRCh37
NC_000002.10:g.241463230T=	NCBI36
NG_008005.1:g.11396T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.712T= MANE Select	ENSP00000302620.3:p.Phe238=
ENST00000307503.3:c.712T=	ENSP00000302620.3:p.Phe238=
ENST00000476698.1:n.364T=
NM_000030.2:c.712T=	NP_000021.1:p.Phe238=
NM_000030.3:c.712T= MANE Select	NP_000021.1:p.Phe238=