Canonical Allele Identifier: CA1339330796
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868985C= , CM000664.2:g.240868985C= GRCh38
NC_000002.11:g.241808402C= , CM000664.1:g.241808402C= GRCh37
NC_000002.10:g.241457075C= NCBI36
NG_008005.1:g.5241C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.120C= MANE Select ENSP00000302620.3:p.Ala40=
ENST00000307503.3:c.120C= ENSP00000302620.3:p.Ala40=
ENST00000472436.1:n.140C=
NM_000030.2:c.120C= NP_000021.1:p.Ala40=
XR_924060.1:n.405+1248G=
NM_000030.3:c.120C= MANE Select NP_000021.1:p.Ala40=