Canonical Allele Identifier: CA645596598

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2028075
• ClinVar RCV Id: RCV002889633
• COSMIC: COSM5752199

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68808446del , CM000678.2:g.68808446del	GRCh38
NC_000016.9:g.68842349del , CM000678.1:g.68842349del	GRCh37
NC_000016.8:g.67399850del	NCBI36
NG_008021.1:g.76155del , LRG_301:g.76155del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.410del MANE Select	ENSP00000261769.4:p.Ala137GlufsTer?
ENST00000261769.9:c.410del	ENSP00000261769.4:p.Ala137GlufsTer?
ENST00000422392.6:c.410del	ENSP00000414946.2:p.Ala137GlufsTer?
ENST00000561751.1:c.177del
ENST00000562836.5:n.481del
ENST00000564676.5:n.692del
ENST00000564745.1:n.405del
ENST00000566510.5:c.410del	ENSP00000458139.1:p.Ala137GlufsTer?
ENST00000566612.5:c.410del	ENSP00000454782.1:p.Ala137GlufsTer?
ENST00000611625.4:c.410del	ENSP00000481063.1:p.Ala137GlufsTer?
ENST00000612417.4:c.410del	ENSP00000478360.1:p.Ala137GlufsTer?
ENST00000621016.4:c.410del	ENSP00000480664.1:p.Ala137GlufsTer?
NM_004360.3:c.410del , LRG_301t1:c.410del	NP_004351.1:p.Ala137GlufsTer?
XM_011523488.1:c.-326del	XP_011521790.1:n.-326del
XM_011523489.1:c.-326del	XP_011521791.1:n.-326del
NM_001317184.1:c.410del	NP_001304113.1:p.Ala137GlufsTer?
NM_001317185.1:c.-1206del	NP_001304114.1:n.-1206del
NM_001317186.1:c.-1410del	NP_001304115.1:n.-1410del
NM_004360.4:c.410del	NP_004351.1:p.Ala137GlufsTer?
NM_004360.5:c.410del MANE Select	NP_004351.1:p.Ala137GlufsTer?
NM_001317184.2:c.410del	NP_001304113.1:p.Ala137GlufsTer?
NM_001317185.2:c.-1206del	NP_001304114.1:n.-1206del
NM_001317186.2:c.-1410del	NP_001304115.1:n.-1410del