Canonical Allele Identifier: CA2839592725
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829777dup , CM000678.2:g.68829777dup GRCh38
NC_000016.9:g.68863680dup , CM000678.1:g.68863680dup GRCh37
NC_000016.8:g.67421181dup NCBI36
NG_008021.1:g.97486dup , LRG_301:g.97486dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2419dup MANE Select ENSP00000261769.4:p.Ile807AsnfsTer6
ENST00000261769.9:c.2419dup ENSP00000261769.4:p.Ile807AsnfsTer6
ENST00000422392.6:c.2236dup ENSP00000414946.2:p.Ile746AsnfsTer6
ENST00000562118.1:n.637dup
ENST00000562836.5:n.2490dup
ENST00000566510.5:c.*1085dup ENSP00000458139.1:n.*1085dup
ENST00000566612.5:c.*659dup ENSP00000454782.1:n.*659dup
ENST00000611625.4:c.2482dup ENSP00000481063.1:p.Ile828AsnfsTer6
ENST00000612417.4:c.1853+3223dup ENSP00000478360.1:n.1853+3223dup
ENST00000621016.4:c.1866-4426dup ENSP00000480664.1:n.1866-4426dup
NM_004360.3:c.2419dup , LRG_301t1:c.2419dup NP_004351.1:p.Ile807AsnfsTer6
XM_011523488.1:c.1684dup XP_011521790.1:p.Ile562AsnfsTer6
XM_011523489.1:c.1684dup XP_011521791.1:p.Ile562AsnfsTer6
NM_001317184.1:c.2236dup NP_001304113.1:p.Ile746AsnfsTer6
NM_001317185.1:c.871dup NP_001304114.1:p.Ile291AsnfsTer6
NM_001317186.1:c.454dup NP_001304115.1:p.Ile152AsnfsTer6
NM_004360.4:c.2419dup NP_004351.1:p.Ile807AsnfsTer6
NM_004360.5:c.2419dup MANE Select NP_004351.1:p.Ile807AsnfsTer6
NM_001317184.2:c.2236dup NP_001304113.1:p.Ile746AsnfsTer6
NM_001317185.2:c.871dup NP_001304114.1:p.Ile291AsnfsTer6
NM_001317186.2:c.454dup NP_001304115.1:p.Ile152AsnfsTer6