Canonical Allele Identifier: CA396472104
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68867237T>G (hg19) chr16:g.68833334T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833334T>G , CM000678.2:g.68833334T>G GRCh38
NC_000016.9:g.68867237T>G , CM000678.1:g.68867237T>G GRCh37
NC_000016.8:g.67424738T>G NCBI36
NG_008021.1:g.101043T>G , LRG_301:g.101043T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2484T>G MANE Select ENSP00000261769.4:p.Asp828Glu
ENST00000261769.9:c.2484T>G ENSP00000261769.4:p.Asp828Glu
ENST00000422392.6:c.2301T>G ENSP00000414946.2:p.Asp767Glu
ENST00000562118.1:n.702T>G
ENST00000562836.5:n.2555T>G
ENST00000566510.5:c.*1150T>G ENSP00000458139.1:n.*1150T>G
ENST00000566612.5:c.*724T>G ENSP00000454782.1:n.*724T>G
ENST00000611625.4:c.2547T>G ENSP00000481063.1:p.Asp849Glu
ENST00000612417.4:c.1854-857T>G ENSP00000478360.1:n.1854-857T>G
ENST00000621016.4:c.1866-869T>G ENSP00000480664.1:n.1866-869T>G
NM_004360.3:c.2484T>G , LRG_301t1:c.2484T>G NP_004351.1:p.Asp828Glu
XM_011523488.1:c.1749T>G XP_011521790.1:p.Asp583Glu
XM_011523489.1:c.1749T>G XP_011521791.1:p.Asp583Glu
NM_001317184.1:c.2301T>G NP_001304113.1:p.Asp767Glu
NM_001317185.1:c.936T>G NP_001304114.1:p.Asp312Glu
NM_001317186.1:c.519T>G NP_001304115.1:p.Asp173Glu
NM_004360.4:c.2484T>G NP_004351.1:p.Asp828Glu
NM_004360.5:c.2484T>G MANE Select NP_004351.1:p.Asp828Glu
NM_001317184.2:c.2301T>G NP_001304113.1:p.Asp767Glu
NM_001317185.2:c.936T>G NP_001304114.1:p.Asp312Glu
NM_001317186.2:c.519T>G NP_001304115.1:p.Asp173Glu
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