Canonical Allele Identifier: CA1339331001
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869326_240869327delinsTG , CM000664.2:g.240869326_240869327delinsTG GRCh38
NC_000002.11:g.241808743_241808744delinsTG , CM000664.1:g.241808743_241808744delinsTG GRCh37
NC_000002.10:g.241457416_241457417delinsTG NCBI36
NG_008005.1:g.5582_5583delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.322_323delinsTG MANE Select ENSP00000302620.3:p.Trp108=
ENST00000307503.3:c.322_323delinsTG ENSP00000302620.3:p.Trp108=
ENST00000472436.1:n.342_343delinsTG
NM_000030.2:c.322_323delinsTG NP_000021.1:p.Trp108=
XR_924060.1:n.405+906_405+907delinsCA
NM_000030.3:c.322_323delinsTG MANE Select NP_000021.1:p.Trp108=