Canonical Allele Identifier: CA396472616
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1793533
ClinVar RCV Id: RCV002426153
dbSNP Id: rs2152144154
MyVariant Identifiers: chr16:g.68867345A>T (hg19) chr16:g.68833442A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833442A>T , CM000678.2:g.68833442A>T GRCh38
NC_000016.9:g.68867345A>T , CM000678.1:g.68867345A>T GRCh37
NC_000016.8:g.67424846A>T NCBI36
NG_008021.1:g.101151A>T , LRG_301:g.101151A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2592A>T MANE Select ENSP00000261769.4:p.Glu864Asp
ENST00000261769.9:c.2592A>T ENSP00000261769.4:p.Glu864Asp
ENST00000422392.6:c.2409A>T ENSP00000414946.2:p.Glu803Asp
ENST00000562118.1:n.810A>T
ENST00000562836.5:n.2663A>T
ENST00000566510.5:c.*1258A>T ENSP00000458139.1:n.*1258A>T
ENST00000566612.5:c.*832A>T ENSP00000454782.1:n.*832A>T
ENST00000611625.4:c.2655A>T ENSP00000481063.1:p.Glu885Asp
ENST00000612417.4:c.1854-749A>T ENSP00000478360.1:n.1854-749A>T
ENST00000621016.4:c.1866-761A>T ENSP00000480664.1:n.1866-761A>T
NM_004360.3:c.2592A>T , LRG_301t1:c.2592A>T NP_004351.1:p.Glu864Asp
XM_011523488.1:c.1857A>T XP_011521790.1:p.Glu619Asp
XM_011523489.1:c.1857A>T XP_011521791.1:p.Glu619Asp
NM_001317184.1:c.2409A>T NP_001304113.1:p.Glu803Asp
NM_001317185.1:c.1044A>T NP_001304114.1:p.Glu348Asp
NM_001317186.1:c.627A>T NP_001304115.1:p.Glu209Asp
NM_004360.4:c.2592A>T NP_004351.1:p.Glu864Asp
NM_004360.5:c.2592A>T MANE Select NP_004351.1:p.Glu864Asp
NM_001317184.2:c.2409A>T NP_001304113.1:p.Glu803Asp
NM_001317185.2:c.1044A>T NP_001304114.1:p.Glu348Asp
NM_001317186.2:c.627A>T NP_001304115.1:p.Glu209Asp
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