Canonical Allele Identifier: CA2732908940

Gene: CDH1

Linked Data

• dbSNP Id: rs2152144045

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833394del , CM000678.2:g.68833394del	GRCh38
NC_000016.9:g.68867297del , CM000678.1:g.68867297del	GRCh37
NC_000016.8:g.67424798del	NCBI36
NG_008021.1:g.101103del , LRG_301:g.101103del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2544del MANE Select	ENSP00000261769.4:p.Asn849ThrfsTer14
ENST00000261769.9:c.2544del	ENSP00000261769.4:p.Asn849ThrfsTer14
ENST00000422392.6:c.2361del	ENSP00000414946.2:p.Asn788ThrfsTer14
ENST00000562118.1:n.762del
ENST00000562836.5:n.2615del
ENST00000566510.5:c.*1210del	ENSP00000458139.1:n.*1210del
ENST00000566612.5:c.*784del	ENSP00000454782.1:n.*784del
ENST00000611625.4:c.2607del	ENSP00000481063.1:p.Asn870ThrfsTer14
ENST00000612417.4:c.1854-797del	ENSP00000478360.1:n.1854-797del
ENST00000621016.4:c.1866-809del	ENSP00000480664.1:n.1866-809del
NM_004360.3:c.2544del , LRG_301t1:c.2544del	NP_004351.1:p.Asn849ThrfsTer14
XM_011523488.1:c.1809del	XP_011521790.1:p.Asn604ThrfsTer14
XM_011523489.1:c.1809del	XP_011521791.1:p.Asn604ThrfsTer14
NM_001317184.1:c.2361del	NP_001304113.1:p.Asn788ThrfsTer14
NM_001317185.1:c.996del	NP_001304114.1:p.Asn333ThrfsTer14
NM_001317186.1:c.579del	NP_001304115.1:p.Asn194ThrfsTer14
NM_004360.4:c.2544del	NP_004351.1:p.Asn849ThrfsTer14
NM_004360.5:c.2544del MANE Select	NP_004351.1:p.Asn849ThrfsTer14
NM_001317184.2:c.2361del	NP_001304113.1:p.Asn788ThrfsTer14
NM_001317185.2:c.996del	NP_001304114.1:p.Asn333ThrfsTer14
NM_001317186.2:c.579del	NP_001304115.1:p.Asn194ThrfsTer14