Canonical Allele Identifier: CA2277257365
Gene: CANT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78992621_78992622delinsAG , CM000679.2:g.78992621_78992622delinsAG GRCh38
NC_000017.10:g.76988703_76988704delinsAG , CM000679.1:g.76988703_76988704delinsAG GRCh37
NC_000017.9:g.74500298_74500299delinsAG NCBI36
NG_016645.1:g.22196_22197delinsCT

Transcript Alleles

HGVS Amino-acid Change
NM_001159773.2:c.*928_*929delinsCT MANE Select NP_001153245.1:n.*928_*929delinsCT
ENST00000392446.10:c.*928_*929delinsCT MANE Select ENSP00000376241.4:n.*928_*929delinsCT
NM_001159772.1:c.*928_*929delinsCT NP_001153244.1:n.*928_*929delinsCT
NM_001159772.2:c.*928_*929delinsCT NP_001153244.1:n.*928_*929delinsCT
NM_001159773.1:c.*928_*929delinsCT NP_001153245.1:n.*928_*929delinsCT
NM_138793.3:c.*928_*929delinsCT NP_620148.1:n.*928_*929delinsCT
NM_138793.4:c.*928_*929delinsCT NP_620148.1:n.*928_*929delinsCT
ENST00000302345.6:c.*928_*929delinsCT ENSP00000307674.2:n.*928_*929delinsCT
ENST00000392446.9:c.*928_*929delinsCT ENSP00000376241.4:n.*928_*929delinsCT
ENST00000592228.1:c.787_788delinsCT ENSP00000466743.1:p.Leu263=
ENST00000620915.4:c.*928_*929delinsCT ENSP00000477798.1:n.*928_*929delinsCT
XM_005257020.1:c.*928_*929delinsCT XP_005257077.1:n.*928_*929delinsCT
XM_005257021.1:c.*928_*929delinsCT XP_005257078.1:n.*928_*929delinsCT
XM_005257022.1:c.*928_*929delinsCT XP_005257079.1:n.*928_*929delinsCT
XM_006721683.1:c.*928_*929delinsCT XP_006721746.1:n.*928_*929delinsCT
XM_011524291.1:c.*928_*929delinsCT XP_011522593.1:n.*928_*929delinsCT
XM_011524292.1:c.*928_*929delinsCT XP_011522594.1:n.*928_*929delinsCT
XM_011524293.1:c.*928_*929delinsCT XP_011522595.1:n.*928_*929delinsCT
XM_011524294.1:c.*928_*929delinsCT XP_011522596.1:n.*928_*929delinsCT
XM_011524294.2:c.*928_*929delinsCT XP_011522596.1:n.*928_*929delinsCT
XM_011524295.1:c.*928_*929delinsCT XP_011522597.1:n.*928_*929delinsCT
XM_011524295.2:c.*928_*929delinsCT XP_011522597.1:n.*928_*929delinsCT
XM_024450564.1:c.*928_*929delinsCT XP_024306332.1:n.*928_*929delinsCT
XR_001752424.2:n.2578_2579delinsCT
XR_935009.1:n.2516_2517delinsAG