Canonical Allele Identifier: CA2499223675

Gene: CDH1

Linked Data

• ClinVar Variation Id: 1069664
• ClinVar RCV Id: RCV001381592
• dbSNP Id: rs2152142199

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829654del , CM000678.2:g.68829654del	GRCh38
NC_000016.9:g.68863557del , CM000678.1:g.68863557del	GRCh37
NC_000016.8:g.67421058del	NCBI36
NG_008021.1:g.97363del , LRG_301:g.97363del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2296del
ENST00000261769.9:c.2296del
ENST00000422392.6:c.2113del
ENST00000562118.1:n.514del
ENST00000562836.5:n.2367del
ENST00000566510.5:c.*962del
ENST00000566612.5:c.*536del
ENST00000611625.4:c.2359del
ENST00000612417.4:c.1853+3100del	ENSP00000478360.1:n.1853+3100del
ENST00000621016.4:c.1866-4549del	ENSP00000480664.1:n.1866-4549del
NM_004360.3:c.2296del , LRG_301t1:c.2296del
XM_011523488.1:c.1561del
XM_011523489.1:c.1561del
NM_001317184.1:c.2113del
NM_001317185.1:c.748del
NM_001317186.1:c.331del
NM_004360.4:c.2296del
NM_004360.5:c.2296del
NM_001317184.2:c.2113del
NM_001317185.2:c.748del
NM_001317186.2:c.331del