Canonical Allele Identifier: CA186248
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs786201045
COSMIC: COSM19541

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68812135_68812136del , CM000678.2:g.68812135_68812136del GRCh38
NC_000016.9:g.68846038_68846039del , CM000678.1:g.68846038_68846039del GRCh37
NC_000016.8:g.67403539_67403540del NCBI36
NG_008021.1:g.79844_79845del , LRG_301:g.79844_79845del

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1009_1010del
ENST00000261769.9:c.1009_1010del
ENST00000422392.6:c.1009_1010del
ENST00000561751.1:c.631_632del
ENST00000562836.5:n.1080_1081del
ENST00000565810.1:n.53_54del
ENST00000566510.5:c.853_854del
ENST00000566612.5:c.1009_1010del
ENST00000611625.4:c.1009_1010del
ENST00000612417.4:c.1009_1010del
ENST00000621016.4:c.1009_1010del
NM_004360.3:c.1009_1010del , LRG_301t1:c.1009_1010del
XM_011523488.1:c.274_275del
XM_011523489.1:c.274_275del
NM_001317184.1:c.1009_1010del
NM_001317185.1:c.-607_-606del
NM_001317186.1:c.-811_-810del
NM_004360.4:c.1009_1010del
NM_004360.5:c.1009_1010del
NM_001317184.2:c.1009_1010del
NM_001317185.2:c.-607_-606del
NM_001317186.2:c.-811_-810del