Canonical Allele Identifier: CA396467214

Gene: CDH1

Linked Data

• ClinVar Variation Id: 532447
• ClinVar RCV Id: RCV002406376
• dbSNP Id: rs1555516894
• MyVariant Identifiers: chr16:g.68856099C>T (hg19) ; chr16:g.68822196C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822196C>T , CM000678.2:g.68822196C>T	GRCh38
NC_000016.9:g.68856099C>T , CM000678.1:g.68856099C>T	GRCh37
NC_000016.8:g.67413600C>T	NCBI36
NG_008021.1:g.89905C>T , LRG_301:g.89905C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1907C>T MANE Select	ENSP00000261769.4:p.Ala636Val
ENST00000261769.9:c.1907C>T	ENSP00000261769.4:p.Ala636Val
ENST00000422392.6:c.1724C>T	ENSP00000414946.2:p.Ala575Val
ENST00000562836.5:n.1978C>T
ENST00000566510.5:c.*573C>T	ENSP00000458139.1:n.*573C>T
ENST00000566612.5:c.*147C>T	ENSP00000454782.1:n.*147C>T
ENST00000611625.4:c.1970C>T	ENSP00000481063.1:p.Ala657Val
ENST00000612417.4:c.1830+77C>T	ENSP00000478360.1:n.1830+77C>T
ENST00000621016.4:c.1865+42C>T	ENSP00000480664.1:n.1865+42C>T
NM_004360.3:c.1907C>T , LRG_301t1:c.1907C>T	NP_004351.1:p.Ala636Val
XM_011523488.1:c.1172C>T	XP_011521790.1:p.Ala391Val
XM_011523489.1:c.1172C>T	XP_011521791.1:p.Ala391Val
NM_001317184.1:c.1724C>T	NP_001304113.1:p.Ala575Val
NM_001317185.1:c.359C>T	NP_001304114.1:p.Ala120Val
NM_001317186.1:c.-59C>T	NP_001304115.1:n.-59C>T
NM_004360.4:c.1907C>T	NP_004351.1:p.Ala636Val
NM_004360.5:c.1907C>T MANE Select	NP_004351.1:p.Ala636Val
NM_001317184.2:c.1724C>T	NP_001304113.1:p.Ala575Val
NM_001317185.2:c.359C>T	NP_001304114.1:p.Ala120Val
NM_001317186.2:c.-59C>T	NP_001304115.1:n.-59C>T