Canonical Allele Identifier: CA2842955787
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829760dup , CM000678.2:g.68829760dup GRCh38
NC_000016.9:g.68863663dup , CM000678.1:g.68863663dup GRCh37
NC_000016.8:g.67421164dup NCBI36
NG_008021.1:g.97469dup , LRG_301:g.97469dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2402dup MANE Select ENSP00000261769.4:p.Ala802CysfsTer5
ENST00000261769.9:c.2402dup ENSP00000261769.4:p.Ala802CysfsTer5
ENST00000422392.6:c.2219dup ENSP00000414946.2:p.Ala741CysfsTer5
ENST00000562118.1:n.620dup
ENST00000562836.5:n.2473dup
ENST00000566510.5:c.*1068dup ENSP00000458139.1:n.*1068dup
ENST00000566612.5:c.*642dup ENSP00000454782.1:n.*642dup
ENST00000611625.4:c.2465dup ENSP00000481063.1:p.Ala823CysfsTer5
ENST00000612417.4:c.1853+3206dup ENSP00000478360.1:n.1853+3206dup
ENST00000621016.4:c.1866-4443dup ENSP00000480664.1:n.1866-4443dup
NM_004360.3:c.2402dup , LRG_301t1:c.2402dup NP_004351.1:p.Ala802CysfsTer5
XM_011523488.1:c.1667dup XP_011521790.1:p.Ala557CysfsTer5
XM_011523489.1:c.1667dup XP_011521791.1:p.Ala557CysfsTer5
NM_001317184.1:c.2219dup NP_001304113.1:p.Ala741CysfsTer5
NM_001317185.1:c.854dup NP_001304114.1:p.Ala286CysfsTer5
NM_001317186.1:c.437dup NP_001304115.1:p.Ala147CysfsTer5
NM_004360.4:c.2402dup NP_004351.1:p.Ala802CysfsTer5
NM_004360.5:c.2402dup MANE Select NP_004351.1:p.Ala802CysfsTer5
NM_001317184.2:c.2219dup NP_001304113.1:p.Ala741CysfsTer5
NM_001317185.2:c.854dup NP_001304114.1:p.Ala286CysfsTer5
NM_001317186.2:c.437dup NP_001304115.1:p.Ala147CysfsTer5