Canonical Allele Identifier: CA396465082
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1485734
ClinVar RCV Id: RCV002000954
dbSNP Id: rs1961075409
MyVariant Identifiers: chr16:g.68853233C>T (hg19) chr16:g.68819330C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819330C>T , CM000678.2:g.68819330C>T GRCh38
NC_000016.9:g.68853233C>T , CM000678.1:g.68853233C>T GRCh37
NC_000016.8:g.67410734C>T NCBI36
NG_008021.1:g.87039C>T , LRG_301:g.87039C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1616C>T MANE Select ENSP00000261769.4:p.Thr539Ile
ENST00000261769.9:c.1616C>T ENSP00000261769.4:p.Thr539Ile
ENST00000422392.6:c.1433C>T ENSP00000414946.2:p.Thr478Ile
ENST00000562836.5:n.1687C>T
ENST00000566510.5:c.*282C>T ENSP00000458139.1:n.*282C>T
ENST00000566612.5:c.1566-2671C>T ENSP00000454782.1:n.1566-2671C>T
ENST00000611625.4:c.1679C>T ENSP00000481063.1:p.Thr560Ile
ENST00000612417.4:c.1616C>T ENSP00000478360.1:p.Thr539Ile
ENST00000621016.4:c.1616C>T ENSP00000480664.1:p.Thr539Ile
NM_004360.3:c.1616C>T , LRG_301t1:c.1616C>T NP_004351.1:p.Thr539Ile
XM_011523488.1:c.881C>T XP_011521790.1:p.Thr294Ile
XM_011523489.1:c.881C>T XP_011521791.1:p.Thr294Ile
NM_001317184.1:c.1433C>T NP_001304113.1:p.Thr478Ile
NM_001317185.1:c.68C>T NP_001304114.1:p.Thr23Ile
NM_001317186.1:c.-254-2671C>T NP_001304115.1:n.-254-2671C>T
NM_004360.4:c.1616C>T NP_004351.1:p.Thr539Ile
NM_004360.5:c.1616C>T MANE Select NP_004351.1:p.Thr539Ile
NM_001317184.2:c.1433C>T NP_001304113.1:p.Thr478Ile
NM_001317185.2:c.68C>T NP_001304114.1:p.Thr23Ile
NM_001317186.2:c.-254-2671C>T NP_001304115.1:n.-254-2671C>T
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