Canonical Allele Identifier: CA314868
Gene: GATM HGNC NCBI

Linked Data

ClinVar Variation Id: 205613
dbSNP Id: rs148564534

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45369403G>A , CM000677.2:g.45369403G>A GRCh38
NC_000015.9:g.45661601G>A , CM000677.1:g.45661601G>A GRCh37
NC_000015.8:g.43448893G>A NCBI36
NG_011674.1:g.14380C>T
NG_011674.2:g.37915C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000396659.8:c.407C>T MANE Select ENSP00000379895.3:p.Thr136Met
ENST00000674905.1:c.407C>T ENSP00000502176.1:p.Thr136Met
ENST00000675158.1:c.407C>T ENSP00000501737.1:p.Thr136Met
ENST00000675323.1:c.407C>T ENSP00000502445.1:p.Thr136Met
ENST00000675701.1:c.347C>T ENSP00000502671.1:p.Thr116Met
ENST00000675974.1:n.498C>T
ENST00000676090.1:c.*1138C>T ENSP00000501630.1:n.*1138C>T
ENST00000396659.7:c.407C>T ENSP00000379895.3:p.Thr136Met
ENST00000558118.1:c.*212C>T ENSP00000452971.1:n.*212C>T
ENST00000558163.1:c.188C>T ENSP00000453781.1:p.Thr63Met
ENST00000558336.5:c.407C>T ENSP00000454008.1:p.Thr136Met
ENST00000558362.5:n.2063C>T
ENST00000558537.5:c.20C>T ENSP00000453151.1:p.Thr7Met
ENST00000558916.1:n.305C>T
ENST00000559885.1:c.20C>T ENSP00000453087.1:p.Thr7Met
ENST00000561148.5:c.20C>T ENSP00000453860.1:p.Thr7Met
NM_001482.2:c.407C>T NP_001473.1:p.Thr136Met
XM_011521450.1:c.455C>T XP_011519752.1:p.Thr152Met
XM_011521451.1:c.449C>T XP_011519753.1:p.Thr150Met
NM_001321015.1:c.20C>T NP_001307944.1:p.Thr7Met
NM_001482.3:c.407C>T MANE Select NP_001473.1:p.Thr136Met
NM_001321015.2:c.20C>T NP_001307944.1:p.Thr7Met