Canonical Allele Identifier: CA396472197
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68867256T>G (hg19) chr16:g.68833353T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833353T>G , CM000678.2:g.68833353T>G GRCh38
NC_000016.9:g.68867256T>G , CM000678.1:g.68867256T>G GRCh37
NC_000016.8:g.67424757T>G NCBI36
NG_008021.1:g.101062T>G , LRG_301:g.101062T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2503T>G MANE Select ENSP00000261769.4:p.Tyr835Asp
ENST00000261769.9:c.2503T>G ENSP00000261769.4:p.Tyr835Asp
ENST00000422392.6:c.2320T>G ENSP00000414946.2:p.Tyr774Asp
ENST00000562118.1:n.721T>G
ENST00000562836.5:n.2574T>G
ENST00000566510.5:c.*1169T>G ENSP00000458139.1:n.*1169T>G
ENST00000566612.5:c.*743T>G ENSP00000454782.1:n.*743T>G
ENST00000611625.4:c.2566T>G ENSP00000481063.1:p.Tyr856Asp
ENST00000612417.4:c.1854-838T>G ENSP00000478360.1:n.1854-838T>G
ENST00000621016.4:c.1866-850T>G ENSP00000480664.1:n.1866-850T>G
NM_004360.3:c.2503T>G , LRG_301t1:c.2503T>G NP_004351.1:p.Tyr835Asp
XM_011523488.1:c.1768T>G XP_011521790.1:p.Tyr590Asp
XM_011523489.1:c.1768T>G XP_011521791.1:p.Tyr590Asp
NM_001317184.1:c.2320T>G NP_001304113.1:p.Tyr774Asp
NM_001317185.1:c.955T>G NP_001304114.1:p.Tyr319Asp
NM_001317186.1:c.538T>G NP_001304115.1:p.Tyr180Asp
NM_004360.4:c.2503T>G NP_004351.1:p.Tyr835Asp
NM_004360.5:c.2503T>G MANE Select NP_004351.1:p.Tyr835Asp
NM_001317184.2:c.2320T>G NP_001304113.1:p.Tyr774Asp
NM_001317185.2:c.955T>G NP_001304114.1:p.Tyr319Asp
NM_001317186.2:c.538T>G NP_001304115.1:p.Tyr180Asp
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