Canonical Allele Identifier: CA978516245
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1960431298

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68799005dup , CM000678.2:g.68799005dup GRCh38
NC_000016.9:g.68832908dup , CM000678.1:g.68832908dup GRCh37
NC_000016.8:g.67390409dup NCBI36
NG_008021.1:g.66714dup , LRG_301:g.66714dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.164-2665dup MANE Select ENSP00000261769.4:n.164-2665dup
ENST00000261769.9:c.164-2665dup ENSP00000261769.4:n.164-2665dup
ENST00000422392.6:c.164-2665dup ENSP00000414946.2:n.164-2665dup
ENST00000562836.5:n.235-2665dup
ENST00000564676.5:n.446-2665dup
ENST00000564745.1:n.159-2665dup
ENST00000566510.5:c.164-2665dup ENSP00000458139.1:n.164-2665dup
ENST00000566612.5:c.164-2665dup ENSP00000454782.1:n.164-2665dup
ENST00000611625.4:c.164-2665dup ENSP00000481063.1:n.164-2665dup
ENST00000612417.4:c.164-2665dup ENSP00000478360.1:n.164-2665dup
ENST00000621016.4:c.164-2665dup ENSP00000480664.1:n.164-2665dup
NM_004360.3:c.164-2665dup , LRG_301t1:c.164-2665dup NP_004351.1:n.164-2665dup
XM_011523488.1:c.-572-2665dup XP_011521790.1:n.-572-2665dup
XM_011523489.1:c.-572-2665dup XP_011521791.1:n.-572-2665dup
NM_001317184.1:c.164-2665dup NP_001304113.1:n.164-2665dup
NM_001317185.1:c.-1452-2665dup NP_001304114.1:n.-1452-2665dup
NM_001317186.1:c.-1656-2665dup NP_001304115.1:n.-1656-2665dup
NM_004360.4:c.164-2665dup NP_004351.1:n.164-2665dup
NM_004360.5:c.164-2665dup MANE Select NP_004351.1:n.164-2665dup
NM_001317184.2:c.164-2665dup NP_001304113.1:n.164-2665dup
NM_001317185.2:c.-1452-2665dup NP_001304114.1:n.-1452-2665dup
NM_001317186.2:c.-1656-2665dup NP_001304115.1:n.-1656-2665dup