Canonical Allele Identifier: CA645580189
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822153_68822156dup , CM000678.2:g.68822153_68822156dup GRCh38
NC_000016.9:g.68856056_68856059dup , CM000678.1:g.68856056_68856059dup GRCh37
NC_000016.8:g.67413557_67413560dup NCBI36
NG_008021.1:g.89862_89865dup , LRG_301:g.89862_89865dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1864_1867dup MANE Select ENSP00000261769.4:p.Thr623LysfsTer?
ENST00000261769.9:c.1864_1867dup ENSP00000261769.4:p.Thr623LysfsTer?
ENST00000422392.6:c.1681_1684dup ENSP00000414946.2:p.Thr562LysfsTer?
ENST00000562836.5:n.1935_1938dup
ENST00000566510.5:c.*530_*533dup ENSP00000458139.1:n.*530_*533dup
ENST00000566612.5:c.*104_*107dup ENSP00000454782.1:n.*104_*107dup
ENST00000611625.4:c.1927_1930dup ENSP00000481063.1:p.Thr644LysfsTer?
ENST00000612417.4:c.1830+34_1830+37dup ENSP00000478360.1:n.1830+34_1830+37dup
ENST00000621016.4:c.1864_1865+2dup
NM_004360.3:c.1864_1867dup , LRG_301t1:c.1864_1867dup NP_004351.1:p.Thr623LysfsTer?
XM_011523488.1:c.1129_1132dup XP_011521790.1:p.Thr378LysfsTer?
XM_011523489.1:c.1129_1132dup XP_011521791.1:p.Thr378LysfsTer?
NM_001317184.1:c.1681_1684dup NP_001304113.1:p.Thr562LysfsTer?
NM_001317185.1:c.316_319dup NP_001304114.1:p.Thr107LysfsTer?
NM_001317186.1:c.-102_-99dup NP_001304115.1:n.-102_-99dup
NM_004360.4:c.1864_1867dup NP_004351.1:p.Thr623LysfsTer?
NM_004360.5:c.1864_1867dup MANE Select NP_004351.1:p.Thr623LysfsTer?
NM_001317184.2:c.1681_1684dup NP_001304113.1:p.Thr562LysfsTer?
NM_001317185.2:c.316_319dup NP_001304114.1:p.Thr107LysfsTer?
NM_001317186.2:c.-102_-99dup NP_001304115.1:n.-102_-99dup