Canonical Allele Identifier: CA2534988356
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2023313
ClinVar RCV Id: RCV002857857

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829645dup , CM000678.2:g.68829645dup GRCh38
NC_000016.9:g.68863548dup , CM000678.1:g.68863548dup GRCh37
NC_000016.8:g.67421049dup NCBI36
NG_008021.1:g.97354dup , LRG_301:g.97354dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2296-9dup MANE Select ENSP00000261769.4:n.2296-9dup
ENST00000261769.9:c.2296-9dup ENSP00000261769.4:n.2296-9dup
ENST00000422392.6:c.2113-9dup ENSP00000414946.2:n.2113-9dup
ENST00000562118.1:n.514-9dup
ENST00000562836.5:n.2367-9dup
ENST00000566510.5:c.*962-9dup ENSP00000458139.1:n.*962-9dup
ENST00000566612.5:c.*536-9dup ENSP00000454782.1:n.*536-9dup
ENST00000611625.4:c.2359-9dup ENSP00000481063.1:n.2359-9dup
ENST00000612417.4:c.1853+3091dup ENSP00000478360.1:n.1853+3091dup
ENST00000621016.4:c.1866-4558dup ENSP00000480664.1:n.1866-4558dup
NM_004360.3:c.2296-9dup , LRG_301t1:c.2296-9dup NP_004351.1:n.2296-9dup
XM_011523488.1:c.1561-9dup XP_011521790.1:n.1561-9dup
XM_011523489.1:c.1561-9dup XP_011521791.1:n.1561-9dup
NM_001317184.1:c.2113-9dup NP_001304113.1:n.2113-9dup
NM_001317185.1:c.748-9dup NP_001304114.1:n.748-9dup
NM_001317186.1:c.331-9dup NP_001304115.1:n.331-9dup
NM_004360.4:c.2296-9dup NP_004351.1:n.2296-9dup
NM_004360.5:c.2296-9dup MANE Select NP_004351.1:n.2296-9dup
NM_001317184.2:c.2113-9dup NP_001304113.1:n.2113-9dup
NM_001317185.2:c.748-9dup NP_001304114.1:n.748-9dup
NM_001317186.2:c.331-9dup NP_001304115.1:n.331-9dup