Canonical Allele Identifier: CA645569991

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2583212
• ClinVar RCV Id: RCV003336883
• COSMIC: COSM5029217

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738329del , CM000678.2:g.68738329del	GRCh38
NC_000016.9:g.68772232del , CM000678.1:g.68772232del	GRCh37
NC_000016.8:g.67329733del	NCBI36
NG_008021.1:g.6038del , LRG_301:g.6038del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.81del MANE Select	ENSP00000261769.4:p.Cys28AlafsTer28
ENST00000261769.9:c.81del	ENSP00000261769.4:p.Cys28AlafsTer28
ENST00000422392.6:c.81del	ENSP00000414946.2:p.Cys28AlafsTer28
ENST00000566510.5:c.81del	ENSP00000458139.1:p.Cys28AlafsTer28
ENST00000566612.5:c.81del	ENSP00000454782.1:p.Cys28AlafsTer28
ENST00000611625.4:c.81del	ENSP00000481063.1:p.Cys28AlafsTer28
ENST00000612417.4:c.81del	ENSP00000478360.1:p.Cys28AlafsTer28
ENST00000621016.4:c.81del	ENSP00000480664.1:p.Cys28AlafsTer28
NM_004360.3:c.81del , LRG_301t1:c.81del	NP_004351.1:p.Cys28AlafsTer28
NM_001317184.1:c.81del	NP_001304113.1:p.Cys28AlafsTer28
NM_001317185.1:c.-1535del	NP_001304114.1:n.-1535del
NM_001317186.1:c.-1739del	NP_001304115.1:n.-1739del
NM_004360.4:c.81del	NP_004351.1:p.Cys28AlafsTer28
NM_004360.5:c.81del MANE Select	NP_004351.1:p.Cys28AlafsTer28
NM_001317184.2:c.81del	NP_001304113.1:p.Cys28AlafsTer28
NM_001317185.2:c.-1535del	NP_001304114.1:n.-1535del
NM_001317186.2:c.-1739del	NP_001304115.1:n.-1739del