Canonical Allele Identifier: CA496154430
Gene: CDH1 HGNC NCBI

Linked Data

COSMIC: COSM972792
MyVariant Identifiers: chr16:g.68853328del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819426del , CM000678.2:g.68819426del GRCh38
NC_000016.9:g.68853329del , CM000678.1:g.68853329del GRCh37
NC_000016.8:g.67410830del NCBI36
NG_008021.1:g.87135del , LRG_301:g.87135del

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1711+1del
ENST00000261769.9:c.1711+1del
ENST00000422392.6:c.1528+1del
ENST00000562836.5:n.1782+1del
ENST00000566510.5:c.*377+1del
ENST00000566612.5:c.1566-2575del ENSP00000454782.1:n.1566-2575del
ENST00000611625.4:c.1774+1del
ENST00000612417.4:c.1711+1del
ENST00000621016.4:c.1711+1del
NM_004360.3:c.1711+1del , LRG_301t1:c.1711+1del
XM_011523488.1:c.976+1del
XM_011523489.1:c.976+1del
NM_001317184.1:c.1528+1del
NM_001317185.1:c.163+1del
NM_001317186.1:c.-254-2575del NP_001304115.1:n.-254-2575del
NM_004360.4:c.1711+1del
NM_004360.5:c.1711+1del
NM_001317184.2:c.1528+1del
NM_001317185.2:c.163+1del
NM_001317186.2:c.-254-2575del NP_001304115.1:n.-254-2575del