Canonical Allele Identifier: CA496152765
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1757073
ClinVar RCV Id: RCV002367258
dbSNP Id: rs863224398
MyVariant Identifiers: chr16:g.68844120A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810217A>T , CM000678.2:g.68810217A>T GRCh38
NC_000016.9:g.68844120A>T , CM000678.1:g.68844120A>T GRCh37
NC_000016.8:g.67401621A>T NCBI36
NG_008021.1:g.77926A>T , LRG_301:g.77926A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.708A>T MANE Select ENSP00000261769.4:p.Ser236=
ENST00000261769.9:c.708A>T ENSP00000261769.4:p.Ser236=
ENST00000422392.6:c.708A>T ENSP00000414946.2:p.Ser236=
ENST00000561751.1:c.454+1369A>T
ENST00000562836.5:n.779A>T
ENST00000566510.5:c.552A>T ENSP00000458139.1:p.Ser184=
ENST00000566612.5:c.708A>T ENSP00000454782.1:p.Ser236=
ENST00000611625.4:c.708A>T ENSP00000481063.1:p.Ser236=
ENST00000612417.4:c.708A>T ENSP00000478360.1:p.Ser236=
ENST00000621016.4:c.708A>T ENSP00000480664.1:p.Ser236=
NM_004360.3:c.708A>T , LRG_301t1:c.708A>T NP_004351.1:p.Ser236=
XM_011523488.1:c.-28A>T XP_011521790.1:n.-28A>T
XM_011523489.1:c.-28A>T XP_011521791.1:n.-28A>T
NM_001317184.1:c.708A>T NP_001304113.1:p.Ser236=
NM_001317185.1:c.-908A>T NP_001304114.1:n.-908A>T
NM_001317186.1:c.-1112A>T NP_001304115.1:n.-1112A>T
NM_004360.4:c.708A>T NP_004351.1:p.Ser236=
NM_004360.5:c.708A>T MANE Select NP_004351.1:p.Ser236=
NM_001317184.2:c.708A>T NP_001304113.1:p.Ser236=
NM_001317185.2:c.-908A>T NP_001304114.1:n.-908A>T
NM_001317186.2:c.-1112A>T NP_001304115.1:n.-1112A>T