Canonical Allele Identifier: CA2582342546
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2583683
ClinVar RCV Id: RCV003334605

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68738387_68738429del , CM000678.2:g.68738387_68738429del GRCh38
NC_000016.9:g.68772290_68772332del , CM000678.1:g.68772290_68772332del GRCh37
NC_000016.8:g.67329791_67329833del NCBI36
NG_008021.1:g.6096_6138del , LRG_301:g.6096_6138del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.139_163+18del
ENST00000261769.9:c.139_163+18del
ENST00000422392.6:c.139_163+18del
ENST00000566510.5:c.139_163+18del
ENST00000566612.5:c.139_163+18del
ENST00000611625.4:c.139_163+18del
ENST00000612417.4:c.139_163+18del
ENST00000621016.4:c.139_163+18del
NM_004360.3:c.139_163+18del , LRG_301t1:c.139_163+18del
NM_001317184.1:c.139_163+18del
NM_001317185.1:c.-1477_-1453+18del
NM_001317186.1:c.-1681_-1657+18del
NM_004360.4:c.139_163+18del
NM_004360.5:c.139_163+18del
NM_001317184.2:c.139_163+18del
NM_001317185.2:c.-1477_-1453+18del
NM_001317186.2:c.-1681_-1657+18del