Canonical Allele Identifier: CA2580091854

Gene: CDH1

Linked Data

• ClinVar Variation Id: 12252
• ClinVar RCV Id: RCV000013039
• dbSNP Id: rs2152143625

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68832894_68833723delinsGGA , CM000678.2:g.68832894_68833723delinsGGA	GRCh38
NC_000016.9:g.68866797_68867626delinsGGA , CM000678.1:g.68866797_68867626delinsGGA	GRCh37
NC_000016.8:g.67424298_67425127delinsGGA	NCBI36
NG_008021.1:g.100603_101432delinsGGA , LRG_301:g.100603_101432delinsGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2440-396_*224delinsGGA
ENST00000261769.9:c.2440-396_*224delinsGGA
ENST00000566612.5:c.*680-396_*1113delinsGGA
ENST00000611625.4:c.2503-396_*224delinsGGA
ENST00000612417.4:c.1854-1297_1854-468delinsGGA	ENSP00000478360.1:n.1854-1297_1854-468delinsGGA
ENST00000621016.4:c.1866-1309_1866-480delinsGGA	ENSP00000480664.1:n.1866-1309_1866-480delinsGGA
NM_004360.3:c.2440-396_*224delinsGGA , LRG_301t1:c.2440-396_*224delinsGGA
XM_011523488.1:c.1705-396_*224delinsGGA
XM_011523489.1:c.1705-396_*224delinsGGA
NM_001317184.1:c.2257-396_*224delinsGGA
NM_001317185.1:c.892-396_*224delinsGGA
NM_001317186.1:c.475-396_*224delinsGGA
NM_004360.4:c.2440-396_*224delinsGGA
NM_004360.5:c.2440-396_*224delinsGGA
NM_001317184.2:c.2257-396_*224delinsGGA
NM_001317185.2:c.892-396_*224delinsGGA
NM_001317186.2:c.475-396_*224delinsGGA