Canonical Allele Identifier: CA2582342547
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2583796
ClinVar RCV Id: RCV003334718

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68738400_68738422del , CM000678.2:g.68738400_68738422del GRCh38
NC_000016.9:g.68772303_68772325del , CM000678.1:g.68772303_68772325del GRCh37
NC_000016.8:g.67329804_67329826del NCBI36
NG_008021.1:g.6109_6131del , LRG_301:g.6109_6131del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.152_163+11del
ENST00000261769.9:c.152_163+11del
ENST00000422392.6:c.152_163+11del
ENST00000566510.5:c.152_163+11del
ENST00000566612.5:c.152_163+11del
ENST00000611625.4:c.152_163+11del
ENST00000612417.4:c.152_163+11del
ENST00000621016.4:c.152_163+11del
NM_004360.3:c.152_163+11del , LRG_301t1:c.152_163+11del
NM_001317184.1:c.152_163+11del
NM_001317185.1:c.-1464_-1453+11del
NM_001317186.1:c.-1668_-1657+11del
NM_004360.4:c.152_163+11del
NM_004360.5:c.152_163+11del
NM_001317184.2:c.152_163+11del
NM_001317185.2:c.-1464_-1453+11del
NM_001317186.2:c.-1668_-1657+11del