Canonical Allele Identifier: CA1139664770

Gene: CDH1

Linked Data

• ClinVar Variation Id: 936565
• ClinVar RCV Id: RCV001205388

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68828308_68831140del , CM000678.2:g.68828308_68831140del	GRCh38
NC_000016.9:g.68862211_68865043del , CM000678.1:g.68862211_68865043del	GRCh37
NC_000016.8:g.67419712_67422544del	NCBI36
NG_008021.1:g.96017_98849del , LRG_301:g.96017_98849del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2295+4_2439+1343del
ENST00000261769.9:c.2295+4_2439+1343del
ENST00000422392.6:c.2112+4_2256+1343del
ENST00000562118.1:n.513+4_657+1343del
ENST00000562836.5:n.2366+4_2510+1343del
ENST00000566510.5:c.*961+4_*1105+1343del
ENST00000566612.5:c.*535+4_*679+1343del
ENST00000611625.4:c.2358+4_2502+1343del
ENST00000612417.4:c.1853+1754_1854-3051del	ENSP00000478360.1:n.1853+1754_1854-3051de...
ENST00000621016.4:c.1866-5895_1866-3063del	ENSP00000480664.1:n.1866-5895_1866-3063de...
NM_004360.3:c.2295+4_2439+1343del , LRG_301t1:c.2295+4_2439+1343del
XM_011523488.1:c.1560+4_1704+1343del
XM_011523489.1:c.1560+4_1704+1343del
NM_001317184.1:c.2112+4_2256+1343del
NM_001317185.1:c.747+4_891+1343del
NM_001317186.1:c.330+4_474+1343del
NM_004360.4:c.2295+4_2439+1343del
NM_004360.5:c.2295+4_2439+1343del
NM_001317184.2:c.2112+4_2256+1343del
NM_001317185.2:c.747+4_891+1343del
NM_001317186.2:c.330+4_474+1343del