Canonical Allele Identifier: CA2499223679

Gene: CDH1

Linked Data

• ClinVar Variation Id: 1050280
• ClinVar RCV Id: RCV001357467
• dbSNP Id: rs2152143824

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833288_68833500del , CM000678.2:g.68833288_68833500del	GRCh38
NC_000016.9:g.68867191_68867403del , CM000678.1:g.68867191_68867403del	GRCh37
NC_000016.8:g.67424692_67424904del	NCBI36
NG_008021.1:g.100997_101209del , LRG_301:g.100997_101209del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2440-2_*1del
ENST00000261769.9:c.2440-2_*1del
ENST00000422392.6:c.2257-2_*1del
ENST00000562118.1:n.658-2_868del
ENST00000562836.5:n.2511-2_2721del
ENST00000566510.5:c.*1106-2_*1316del
ENST00000566612.5:c.*680-2_*890del
ENST00000611625.4:c.2503-2_*1del
ENST00000612417.4:c.1854-903_1854-691del	ENSP00000478360.1:n.1854-903_1854-691del
ENST00000621016.4:c.1866-915_1866-703del	ENSP00000480664.1:n.1866-915_1866-703del
NM_004360.3:c.2440-2_*1del , LRG_301t1:c.2440-2_*1del
XM_011523488.1:c.1705-2_*1del
XM_011523489.1:c.1705-2_*1del
NM_001317184.1:c.2257-2_*1del
NM_001317185.1:c.892-2_*1del
NM_001317186.1:c.475-2_*1del
NM_004360.4:c.2440-2_*1del
NM_004360.5:c.2440-2_*1del
NM_001317184.2:c.2257-2_*1del
NM_001317185.2:c.892-2_*1del
NM_001317186.2:c.475-2_*1del