Canonical Allele Identifier: CA129620
Gene: CANT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78997395dup , CM000679.2:g.78997395dup GRCh38
NC_000017.10:g.76993477dup , CM000679.1:g.76993477dup GRCh37
NC_000017.9:g.74505072dup NCBI36
NG_016645.1:g.17423dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000392446.10:c.228dup MANE Select ENSP00000376241.4:p.Trp77LeufsTer13
ENST00000302345.6:c.228dup ENSP00000307674.2:p.Trp77LeufsTer13
ENST00000392446.9:c.228dup ENSP00000376241.4:p.Trp77LeufsTer13
ENST00000588075.5:c.228dup
ENST00000588611.5:c.133-66dup ENSP00000465816.1:n.133-66dup
ENST00000591773.5:c.228dup ENSP00000467437.1:p.Trp77LeufsTer13
ENST00000592228.1:c.228dup ENSP00000466743.1:p.Trp77LeufsTer13
ENST00000620915.4:c.228dup ENSP00000477798.1:p.Trp77LeufsTer13
NM_001159772.1:c.228dup NP_001153244.1:p.Trp77LeufsTer13
NM_001159773.1:c.228dup NP_001153245.1:p.Trp77LeufsTer13
NM_138793.3:c.228dup NP_620148.1:p.Trp77LeufsTer13
XM_005257020.1:c.228dup XP_005257077.1:p.Trp77LeufsTer13
XM_005257021.1:c.228dup XP_005257078.1:p.Trp77LeufsTer13
XM_005257022.1:c.228dup XP_005257079.1:p.Trp77LeufsTer13
XM_006721683.1:c.228dup XP_006721746.1:p.Trp77LeufsTer13
XM_011524291.1:c.228dup XP_011522593.1:p.Trp77LeufsTer13
XM_011524292.1:c.228dup XP_011522594.1:p.Trp77LeufsTer13
XM_011524293.1:c.228dup XP_011522595.1:p.Trp77LeufsTer13
XM_011524294.1:c.228dup XP_011522596.1:p.Trp77LeufsTer13
XM_011524295.1:c.228dup XP_011522597.1:p.Trp77LeufsTer13
XM_011524294.2:c.228dup XP_011522596.1:p.Trp77LeufsTer13
XM_011524295.2:c.228dup XP_011522597.1:p.Trp77LeufsTer13
XM_024450564.1:c.228dup XP_024306332.1:p.Trp77LeufsTer13
XR_001752424.2:n.672dup
NM_001159773.2:c.228dup MANE Select NP_001153245.1:p.Trp77LeufsTer13
NM_001159772.2:c.228dup NP_001153244.1:p.Trp77LeufsTer13
NM_138793.4:c.228dup NP_620148.1:p.Trp77LeufsTer13