Canonical Allele Identifier: CA658683940

Gene: CDH1

Linked Data

• ClinVar Variation Id: 491542
• ClinVar RCV Id: RCV000583500 ; RCV001211016
• dbSNP Id: rs1555509656

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737468_68737469delinsGT , CM000678.2:g.68737468_68737469delinsGT	GRCh38
NC_000016.9:g.68771371_68771372delinsGT , CM000678.1:g.68771371_68771372delinsGT	GRCh37
NC_000016.8:g.67328872_67328873delinsGT	NCBI36
NG_008021.1:g.5177_5178delinsGT , LRG_301:g.5177_5178delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.48+5_48+6delinsGT MANE Select	ENSP00000261769.4:n.48+5_48+6delinsGT
ENST00000261769.9:c.48+5_48+6delinsGT	ENSP00000261769.4:n.48+5_48+6delinsGT
ENST00000422392.6:c.48+5_48+6delinsGT	ENSP00000414946.2:n.48+5_48+6delinsGT
ENST00000566510.5:c.48+5_48+6delinsGT	ENSP00000458139.1:n.48+5_48+6delinsGT
ENST00000566612.5:c.48+5_48+6delinsGT	ENSP00000454782.1:n.48+5_48+6delinsGT
ENST00000611625.4:c.48+5_48+6delinsGT	ENSP00000481063.1:n.48+5_48+6delinsGT
ENST00000612417.4:c.48+5_48+6delinsGT	ENSP00000478360.1:n.48+5_48+6delinsGT
ENST00000621016.4:c.48+5_48+6delinsGT	ENSP00000480664.1:n.48+5_48+6delinsGT
NM_004360.3:c.48+5_48+6delinsGT , LRG_301t1:c.48+5_48+6delinsGT	NP_004351.1:n.48+5_48+6delinsGT
NM_001317184.1:c.48+5_48+6delinsGT	NP_001304113.1:n.48+5_48+6delinsGT
NM_001317185.1:c.-1568+5_-1568+6delinsGT	NP_001304114.1:n.-1568+5_-1568+6delinsGT
NM_001317186.1:c.-1772+5_-1772+6delinsGT	NP_001304115.1:n.-1772+5_-1772+6delinsGT
NM_004360.4:c.48+5_48+6delinsGT	NP_004351.1:n.48+5_48+6delinsGT
NM_004360.5:c.48+5_48+6delinsGT MANE Select	NP_004351.1:n.48+5_48+6delinsGT
NM_001317184.2:c.48+5_48+6delinsGT	NP_001304113.1:n.48+5_48+6delinsGT
NM_001317185.2:c.-1568+5_-1568+6delinsGT	NP_001304114.1:n.-1568+5_-1568+6delinsGT
NM_001317186.2:c.-1772+5_-1772+6delinsGT	NP_001304115.1:n.-1772+5_-1772+6delinsGT