Canonical Allele Identifier: CA8129773
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 803264
ClinVar RCV Id: RCV000989616
dbSNP Id: rs587782476

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737459_68737461del , CM000678.2:g.68737459_68737461del GRCh38
NC_000016.9:g.68771362_68771364del , CM000678.1:g.68771362_68771364del GRCh37
NC_000016.8:g.67328863_67328865del NCBI36
NG_008021.1:g.5168_5170del , LRG_301:g.5168_5170del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.44_46del MANE Select ENSP00000261769.4:p.Leu15del
ENST00000261769.9:c.44_46del ENSP00000261769.4:p.Leu15del
ENST00000422392.6:c.44_46del ENSP00000414946.2:p.Leu15del
ENST00000566510.5:c.44_46del ENSP00000458139.1:p.Leu15del
ENST00000566612.5:c.44_46del ENSP00000454782.1:p.Leu15del
ENST00000611625.4:c.44_46del ENSP00000481063.1:p.Leu15del
ENST00000612417.4:c.44_46del ENSP00000478360.1:p.Leu15del
ENST00000621016.4:c.44_46del ENSP00000480664.1:p.Leu15del
NM_004360.3:c.44_46del , LRG_301t1:c.44_46del NP_004351.1:p.Leu15del
NM_001317184.1:c.44_46del NP_001304113.1:p.Leu15del
NM_001317185.1:c.-1572_-1570del NP_001304114.1:n.-1572_-1570del
NM_001317186.1:c.-1776_-1774del NP_001304115.1:n.-1776_-1774del
NM_004360.4:c.44_46del NP_004351.1:p.Leu15del
NM_004360.5:c.44_46del MANE Select NP_004351.1:p.Leu15del
NM_001317184.2:c.44_46del NP_001304113.1:p.Leu15del
NM_001317185.2:c.-1572_-1570del NP_001304114.1:n.-1572_-1570del
NM_001317186.2:c.-1776_-1774del NP_001304115.1:n.-1776_-1774del