Canonical Allele Identifier: CA2640214147
Gene: CANT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78993990_78993991insCA , CM000679.2:g.78993990_78993991insCA GRCh38
NC_000017.10:g.76990072_76990073insCA , CM000679.1:g.76990072_76990073insCA GRCh37
NC_000017.9:g.74501667_74501668insCA NCBI36
NG_016645.1:g.20827_20828insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000392446.10:c.836-71_836-70insTG MANE Select ENSP00000376241.4:n.836-71_836-70insTG
ENST00000302345.6:c.836-71_836-70insTG ENSP00000307674.2:n.836-71_836-70insTG
ENST00000392446.9:c.836-71_836-70insTG ENSP00000376241.4:n.836-71_836-70insTG
ENST00000588096.1:n.233-71_233-70insTG
ENST00000591773.5:c.836-71_836-70insTG ENSP00000467437.1:n.836-71_836-70insTG
ENST00000592228.1:c.648-1230_648-1229insTG ENSP00000466743.1:n.648-1230_648-1229insTG
ENST00000620915.4:c.836-71_836-70insTG ENSP00000477798.1:n.836-71_836-70insTG
NM_001159772.1:c.836-71_836-70insTG NP_001153244.1:n.836-71_836-70insTG
NM_001159773.1:c.836-71_836-70insTG NP_001153245.1:n.836-71_836-70insTG
NM_138793.3:c.836-71_836-70insTG NP_620148.1:n.836-71_836-70insTG
XM_005257020.1:c.836-71_836-70insTG XP_005257077.1:n.836-71_836-70insTG
XM_005257021.1:c.836-71_836-70insTG XP_005257078.1:n.836-71_836-70insTG
XM_005257022.1:c.836-71_836-70insTG XP_005257079.1:n.836-71_836-70insTG
XM_006721683.1:c.836-71_836-70insTG XP_006721746.1:n.836-71_836-70insTG
XM_011524291.1:c.836-71_836-70insTG XP_011522593.1:n.836-71_836-70insTG
XM_011524292.1:c.836-71_836-70insTG XP_011522594.1:n.836-71_836-70insTG
XM_011524293.1:c.836-71_836-70insTG XP_011522595.1:n.836-71_836-70insTG
XM_011524294.1:c.836-71_836-70insTG XP_011522596.1:n.836-71_836-70insTG
XM_011524295.1:c.836-71_836-70insTG XP_011522597.1:n.836-71_836-70insTG
XM_011524294.2:c.836-71_836-70insTG XP_011522596.1:n.836-71_836-70insTG
XM_011524295.2:c.836-71_836-70insTG XP_011522597.1:n.836-71_836-70insTG
XM_024450564.1:c.836-71_836-70insTG XP_024306332.1:n.836-71_836-70insTG
XR_001752424.2:n.1280-71_1280-70insTG
NM_001159773.2:c.836-71_836-70insTG MANE Select NP_001153245.1:n.836-71_836-70insTG
NM_001159772.2:c.836-71_836-70insTG NP_001153244.1:n.836-71_836-70insTG
NM_138793.4:c.836-71_836-70insTG NP_620148.1:n.836-71_836-70insTG