Canonical Allele Identifier: CA2586971644
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877591_240877593delinsGCG , CM000664.2:g.240877591_240877593delinsGCG GRCh38
NC_000002.11:g.241817008_241817010delinsGCG , CM000664.1:g.241817008_241817010delinsGCG GRCh37
NC_000002.10:g.241465681_241465683delinsGCG NCBI36
NG_008005.1:g.13847_13849delinsGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.901_903delinsGCG MANE Select ENSP00000302620.3:p.Arg301Ala
ENST00000307503.3:c.901_903delinsGCG ENSP00000302620.3:p.Arg301Ala
ENST00000470255.1:n.679_681delinsGCG
NM_000030.2:c.901_903delinsGCG NP_000021.1:p.Arg301Ala
NM_000030.3:c.901_903delinsGCG MANE Select NP_000021.1:p.Arg301Ala