Canonical Allele Identifier: CA314876
Community Standard Title: NM_001482.3(GATM):c.778C>T (p.Arg260Ter)
Gene: GATM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45366406G>A , CM000677.2:g.45366406G>A GRCh38
NC_000015.9:g.45658604G>A , CM000677.1:g.45658604G>A GRCh37
NC_000015.8:g.43445896G>A NCBI36
NG_011674.1:g.17377C>T
NG_011674.2:g.40912C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001482.3:c.778C>T MANE Select NP_001473.1:p.Arg260Ter
ENST00000396659.8:c.778C>T MANE Select ENSP00000379895.3:p.Arg260Ter
NM_001321015.1:c.391C>T NP_001307944.1:p.Arg131Ter
NM_001321015.2:c.391C>T NP_001307944.1:p.Arg131Ter
NM_001482.2:c.778C>T NP_001473.1:p.Arg260Ter
ENST00000396659.7:c.778C>T ENSP00000379895.3:p.Arg260Ter
ENST00000558336.5:c.778C>T ENSP00000454008.1:p.Arg260Ter
ENST00000558362.5:n.2434C>T
ENST00000558916.1:n.676C>T
ENST00000674905.1:c.778C>T ENSP00000502176.1:p.Arg260Ter
ENST00000675158.1:c.778C>T ENSP00000501737.1:p.Arg260Ter
ENST00000675323.1:c.778C>T ENSP00000502445.1:p.Arg260Ter
ENST00000675701.1:c.718C>T ENSP00000502671.1:p.Arg240Ter
ENST00000675974.1:n.869C>T
ENST00000676090.1:c.*1509C>T ENSP00000501630.1:n.*1509C>T
XM_011521450.1:c.826C>T XP_011519752.1:p.Arg276Ter
XM_011521451.1:c.820C>T XP_011519753.1:p.Arg274Ter
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