Canonical Allele Identifier: CA1339335517

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240877571C= , CM000664.2:g.240877571C=	GRCh38
NC_000002.11:g.241816988C= , CM000664.1:g.241816988C=	GRCh37
NC_000002.10:g.241465661C=	NCBI36
NG_008005.1:g.13827C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000307503.4:c.881C= MANE Select	ENSP00000302620.3:p.Ala294=
ENST00000307503.3:c.881C=	ENSP00000302620.3:p.Ala294=
ENST00000470255.1:n.659C=
NM_000030.2:c.881C=	NP_000021.1:p.Ala294=
NM_000030.3:c.881C= MANE Select	NP_000021.1:p.Ala294=