Canonical Allele Identifier: CA496149611

Gene: CDH1

Linked Data

• COSMIC: COSM435584
• MyVariant Identifiers: chr16:g.68772257del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738354del , CM000678.2:g.68738354del	GRCh38
NC_000016.9:g.68772257del , CM000678.1:g.68772257del	GRCh37
NC_000016.8:g.67329758del	NCBI36
NG_008021.1:g.6063del , LRG_301:g.6063del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.106del MANE Select	ENSP00000261769.4:p.Ser36AlafsTer20
ENST00000261769.9:c.106del	ENSP00000261769.4:p.Ser36AlafsTer20
ENST00000422392.6:c.106del	ENSP00000414946.2:p.Ser36AlafsTer20
ENST00000566510.5:c.106del	ENSP00000458139.1:p.Ser36AlafsTer20
ENST00000566612.5:c.106del	ENSP00000454782.1:p.Ser36AlafsTer20
ENST00000611625.4:c.106del	ENSP00000481063.1:p.Ser36AlafsTer20
ENST00000612417.4:c.106del	ENSP00000478360.1:p.Ser36AlafsTer20
ENST00000621016.4:c.106del	ENSP00000480664.1:p.Ser36AlafsTer20
NM_004360.3:c.106del , LRG_301t1:c.106del	NP_004351.1:p.Ser36AlafsTer20
NM_001317184.1:c.106del	NP_001304113.1:p.Ser36AlafsTer20
NM_001317185.1:c.-1510del	NP_001304114.1:n.-1510del
NM_001317186.1:c.-1714del	NP_001304115.1:n.-1714del
NM_004360.4:c.106del	NP_004351.1:p.Ser36AlafsTer20
NM_004360.5:c.106del MANE Select	NP_004351.1:p.Ser36AlafsTer20
NM_001317184.2:c.106del	NP_001304113.1:p.Ser36AlafsTer20
NM_001317185.2:c.-1510del	NP_001304114.1:n.-1510del
NM_001317186.2:c.-1714del	NP_001304115.1:n.-1714del