Canonical Allele Identifier: CA396472745
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1405890
ClinVar RCV Id: RCV001906757
dbSNP Id: rs749203461
MyVariant Identifiers: chr16:g.68867367C>G (hg19) chr16:g.68833464C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833464C>G , CM000678.2:g.68833464C>G GRCh38
NC_000016.9:g.68867367C>G , CM000678.1:g.68867367C>G GRCh37
NC_000016.8:g.67424868C>G NCBI36
NG_008021.1:g.101173C>G , LRG_301:g.101173C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2614C>G MANE Select ENSP00000261769.4:p.Leu872Val
ENST00000261769.9:c.2614C>G ENSP00000261769.4:p.Leu872Val
ENST00000422392.6:c.2431C>G ENSP00000414946.2:p.Leu811Val
ENST00000562118.1:n.832C>G
ENST00000562836.5:n.2685C>G
ENST00000566510.5:c.*1280C>G ENSP00000458139.1:n.*1280C>G
ENST00000566612.5:c.*854C>G ENSP00000454782.1:n.*854C>G
ENST00000611625.4:c.2677C>G ENSP00000481063.1:p.Leu893Val
ENST00000612417.4:c.1854-727C>G ENSP00000478360.1:n.1854-727C>G
ENST00000621016.4:c.1866-739C>G ENSP00000480664.1:n.1866-739C>G
NM_004360.3:c.2614C>G , LRG_301t1:c.2614C>G NP_004351.1:p.Leu872Val
XM_011523488.1:c.1879C>G XP_011521790.1:p.Leu627Val
XM_011523489.1:c.1879C>G XP_011521791.1:p.Leu627Val
NM_001317184.1:c.2431C>G NP_001304113.1:p.Leu811Val
NM_001317185.1:c.1066C>G NP_001304114.1:p.Leu356Val
NM_001317186.1:c.649C>G NP_001304115.1:p.Leu217Val
NM_004360.4:c.2614C>G NP_004351.1:p.Leu872Val
NM_004360.5:c.2614C>G MANE Select NP_004351.1:p.Leu872Val
NM_001317184.2:c.2431C>G NP_001304113.1:p.Leu811Val
NM_001317185.2:c.1066C>G NP_001304114.1:p.Leu356Val
NM_001317186.2:c.649C>G NP_001304115.1:p.Leu217Val
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