Canonical Allele Identifier: CA396472366
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1567517746
MyVariant Identifiers: chr16:g.68867295C>G (hg19) chr16:g.68833392C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833392C>G , CM000678.2:g.68833392C>G GRCh38
NC_000016.9:g.68867295C>G , CM000678.1:g.68867295C>G GRCh37
NC_000016.8:g.67424796C>G NCBI36
NG_008021.1:g.101101C>G , LRG_301:g.101101C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2542C>G MANE Select ENSP00000261769.4:p.Leu848Val
ENST00000261769.9:c.2542C>G ENSP00000261769.4:p.Leu848Val
ENST00000422392.6:c.2359C>G ENSP00000414946.2:p.Leu787Val
ENST00000562118.1:n.760C>G
ENST00000562836.5:n.2613C>G
ENST00000566510.5:c.*1208C>G ENSP00000458139.1:n.*1208C>G
ENST00000566612.5:c.*782C>G ENSP00000454782.1:n.*782C>G
ENST00000611625.4:c.2605C>G ENSP00000481063.1:p.Leu869Val
ENST00000612417.4:c.1854-799C>G ENSP00000478360.1:n.1854-799C>G
ENST00000621016.4:c.1866-811C>G ENSP00000480664.1:n.1866-811C>G
NM_004360.3:c.2542C>G , LRG_301t1:c.2542C>G NP_004351.1:p.Leu848Val
XM_011523488.1:c.1807C>G XP_011521790.1:p.Leu603Val
XM_011523489.1:c.1807C>G XP_011521791.1:p.Leu603Val
NM_001317184.1:c.2359C>G NP_001304113.1:p.Leu787Val
NM_001317185.1:c.994C>G NP_001304114.1:p.Leu332Val
NM_001317186.1:c.577C>G NP_001304115.1:p.Leu193Val
NM_004360.4:c.2542C>G NP_004351.1:p.Leu848Val
NM_004360.5:c.2542C>G MANE Select NP_004351.1:p.Leu848Val
NM_001317184.2:c.2359C>G NP_001304113.1:p.Leu787Val
NM_001317185.2:c.994C>G NP_001304114.1:p.Leu332Val
NM_001317186.2:c.577C>G NP_001304115.1:p.Leu193Val
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