Canonical Allele Identifier: CA645596594

Gene: CDH1

Linked Data

• COSMIC: COSM4747419

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801779del , CM000678.2:g.68801779del	GRCh38
NC_000016.9:g.68835682del , CM000678.1:g.68835682del	GRCh37
NC_000016.8:g.67393183del	NCBI36
NG_008021.1:g.69488del , LRG_301:g.69488del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.273del MANE Select	ENSP00000261769.4:p.His92IlefsTer25
ENST00000261769.9:c.273del	ENSP00000261769.4:p.His92IlefsTer25
ENST00000422392.6:c.273del	ENSP00000414946.2:p.His92IlefsTer25
ENST00000561751.1:c.40del
ENST00000562836.5:n.344del
ENST00000564676.5:n.555del
ENST00000564745.1:n.268del
ENST00000566510.5:c.273del	ENSP00000458139.1:p.His92IlefsTer25
ENST00000566612.5:c.273del	ENSP00000454782.1:p.His92IlefsTer25
ENST00000611625.4:c.273del	ENSP00000481063.1:p.His92IlefsTer25
ENST00000612417.4:c.273del	ENSP00000478360.1:p.His92IlefsTer25
ENST00000621016.4:c.273del	ENSP00000480664.1:p.His92IlefsTer25
NM_004360.3:c.273del , LRG_301t1:c.273del	NP_004351.1:p.His92IlefsTer25
XM_011523488.1:c.-463del	XP_011521790.1:n.-463del
XM_011523489.1:c.-463del	XP_011521791.1:n.-463del
NM_001317184.1:c.273del	NP_001304113.1:p.His92IlefsTer25
NM_001317185.1:c.-1343del	NP_001304114.1:n.-1343del
NM_001317186.1:c.-1547del	NP_001304115.1:n.-1547del
NM_004360.4:c.273del	NP_004351.1:p.His92IlefsTer25
NM_004360.5:c.273del MANE Select	NP_004351.1:p.His92IlefsTer25
NM_001317184.2:c.273del	NP_001304113.1:p.His92IlefsTer25
NM_001317185.2:c.-1343del	NP_001304114.1:n.-1343del
NM_001317186.2:c.-1547del	NP_001304115.1:n.-1547del