Canonical Allele Identifier: CA1339334183

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240875145C= , CM000664.2:g.240875145C=	GRCh38
NC_000002.11:g.241814562C= , CM000664.1:g.241814562C=	GRCh37
NC_000002.10:g.241463235C=	NCBI36
NG_008005.1:g.11401C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.717C= MANE Select	ENSP00000302620.3:p.Ser239=
ENST00000307503.3:c.717C=	ENSP00000302620.3:p.Ser239=
ENST00000476698.1:n.369C=
NM_000030.2:c.717C=	NP_000021.1:p.Ser239=
NM_000030.3:c.717C= MANE Select	NP_000021.1:p.Ser239=