Canonical Allele Identifier: CA10577533

Gene: CDH1

Linked Data

• ClinVar Variation Id: 234886
• ClinVar RCV Id: RCV000218039
• dbSNP Id: rs876661278
• MyVariant Identifiers: chr16:g.68772269A>T (hg19) ; chr16:g.68738366A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738366A>T , CM000678.2:g.68738366A>T	GRCh38
NC_000016.9:g.68772269A>T , CM000678.1:g.68772269A>T	GRCh37
NC_000016.8:g.67329770A>T	NCBI36
NG_008021.1:g.6075A>T , LRG_301:g.6075A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.118A>T MANE Select	ENSP00000261769.4:p.Thr40Ser
ENST00000261769.9:c.118A>T	ENSP00000261769.4:p.Thr40Ser
ENST00000422392.6:c.118A>T	ENSP00000414946.2:p.Thr40Ser
ENST00000566510.5:c.118A>T	ENSP00000458139.1:p.Thr40Ser
ENST00000566612.5:c.118A>T	ENSP00000454782.1:p.Thr40Ser
ENST00000611625.4:c.118A>T	ENSP00000481063.1:p.Thr40Ser
ENST00000612417.4:c.118A>T	ENSP00000478360.1:p.Thr40Ser
ENST00000621016.4:c.118A>T	ENSP00000480664.1:p.Thr40Ser
NM_004360.3:c.118A>T , LRG_301t1:c.118A>T	NP_004351.1:p.Thr40Ser
NM_001317184.1:c.118A>T	NP_001304113.1:p.Thr40Ser
NM_001317185.1:c.-1498A>T	NP_001304114.1:n.-1498A>T
NM_001317186.1:c.-1702A>T	NP_001304115.1:n.-1702A>T
NM_004360.4:c.118A>T	NP_004351.1:p.Thr40Ser
NM_004360.5:c.118A>T MANE Select	NP_004351.1:p.Thr40Ser
NM_001317184.2:c.118A>T	NP_001304113.1:p.Thr40Ser
NM_001317185.2:c.-1498A>T	NP_001304114.1:n.-1498A>T
NM_001317186.2:c.-1702A>T	NP_001304115.1:n.-1702A>T