Canonical Allele Identifier: CA8130277
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 259293
dbSNP Id: rs34751606

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829819C>T , CM000678.2:g.68829819C>T GRCh38
NC_000016.9:g.68863722C>T , CM000678.1:g.68863722C>T GRCh37
NC_000016.8:g.67421223C>T NCBI36
NG_008021.1:g.97528C>T , LRG_301:g.97528C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+22C>T MANE Select ENSP00000261769.4:n.2439+22C>T
ENST00000261769.9:c.2439+22C>T ENSP00000261769.4:n.2439+22C>T
ENST00000422392.6:c.2256+22C>T ENSP00000414946.2:n.2256+22C>T
ENST00000562118.1:n.657+22C>T
ENST00000562836.5:n.2510+22C>T
ENST00000566510.5:c.*1105+22C>T ENSP00000458139.1:n.*1105+22C>T
ENST00000566612.5:c.*679+22C>T ENSP00000454782.1:n.*679+22C>T
ENST00000611625.4:c.2502+22C>T ENSP00000481063.1:n.2502+22C>T
ENST00000612417.4:c.1853+3265C>T ENSP00000478360.1:n.1853+3265C>T
ENST00000621016.4:c.1866-4384C>T ENSP00000480664.1:n.1866-4384C>T
NM_004360.3:c.2439+22C>T , LRG_301t1:c.2439+22C>T NP_004351.1:n.2439+22C>T
XM_011523488.1:c.1704+22C>T XP_011521790.1:n.1704+22C>T
XM_011523489.1:c.1704+22C>T XP_011521791.1:n.1704+22C>T
NM_001317184.1:c.2256+22C>T NP_001304113.1:n.2256+22C>T
NM_001317185.1:c.891+22C>T NP_001304114.1:n.891+22C>T
NM_001317186.1:c.474+22C>T NP_001304115.1:n.474+22C>T
NM_004360.4:c.2439+22C>T NP_004351.1:n.2439+22C>T
NM_004360.5:c.2439+22C>T MANE Select NP_004351.1:n.2439+22C>T
NM_001317184.2:c.2256+22C>T NP_001304113.1:n.2256+22C>T
NM_001317185.2:c.891+22C>T NP_001304114.1:n.891+22C>T
NM_001317186.2:c.474+22C>T NP_001304115.1:n.474+22C>T