Canonical Allele Identifier: CA645596630
Gene: CDH1 HGNC NCBI

Linked Data

COSMIC: COSM19785

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810295_68810303delinsT , CM000678.2:g.68810295_68810303delinsT GRCh38
NC_000016.9:g.68844198_68844206delinsT , CM000678.1:g.68844198_68844206delinsT GRCh37
NC_000016.8:g.67401699_67401707delinsT NCBI36
NG_008021.1:g.78004_78012delinsT , LRG_301:g.78004_78012delinsT

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.786_794delinsT MANE Select ENSP00000261769.4:p.Thr263GlyfsTer3
ENST00000261769.9:c.786_794delinsT ENSP00000261769.4:p.Thr263GlyfsTer3
ENST00000422392.6:c.786_794delinsT ENSP00000414946.2:p.Thr263GlyfsTer3
ENST00000561751.1:c.455-1389_455-1381delinsT
ENST00000562836.5:n.857_865delinsT
ENST00000566510.5:c.630_638delinsT ENSP00000458139.1:p.Thr211GlyfsTer3
ENST00000566612.5:c.786_794delinsT ENSP00000454782.1:p.Thr263GlyfsTer3
ENST00000611625.4:c.786_794delinsT ENSP00000481063.1:p.Thr263GlyfsTer3
ENST00000612417.4:c.786_794delinsT ENSP00000478360.1:p.Thr263GlyfsTer3
ENST00000621016.4:c.786_794delinsT ENSP00000480664.1:p.Thr263GlyfsTer3
NM_004360.3:c.786_794delinsT , LRG_301t1:c.786_794delinsT NP_004351.1:p.Thr263GlyfsTer3
XM_011523488.1:c.51_59delinsT XP_011521790.1:p.Thr18GlyfsTer3
XM_011523489.1:c.51_59delinsT XP_011521791.1:p.Thr18GlyfsTer3
NM_001317184.1:c.786_794delinsT NP_001304113.1:p.Thr263GlyfsTer3
NM_001317185.1:c.-830_-822delinsT NP_001304114.1:n.-830_-822delinsT
NM_001317186.1:c.-1034_-1026delinsT NP_001304115.1:n.-1034_-1026delinsT
NM_004360.4:c.786_794delinsT NP_004351.1:p.Thr263GlyfsTer3
NM_004360.5:c.786_794delinsT MANE Select NP_004351.1:p.Thr263GlyfsTer3
NM_001317184.2:c.786_794delinsT NP_001304113.1:p.Thr263GlyfsTer3
NM_001317185.2:c.-830_-822delinsT NP_001304114.1:n.-830_-822delinsT
NM_001317186.2:c.-1034_-1026delinsT NP_001304115.1:n.-1034_-1026delinsT