Canonical Allele Identifier: CA396472288
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs587781300
MyVariant Identifiers: chr16:g.68867272C>A (hg19) chr16:g.68833369C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833369C>A , CM000678.2:g.68833369C>A GRCh38
NC_000016.9:g.68867272C>A , CM000678.1:g.68867272C>A GRCh37
NC_000016.8:g.67424773C>A NCBI36
NG_008021.1:g.101078C>A , LRG_301:g.101078C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2519C>A MANE Select ENSP00000261769.4:p.Ser840Tyr
ENST00000261769.9:c.2519C>A ENSP00000261769.4:p.Ser840Tyr
ENST00000422392.6:c.2336C>A ENSP00000414946.2:p.Ser779Tyr
ENST00000562118.1:n.737C>A
ENST00000562836.5:n.2590C>A
ENST00000566510.5:c.*1185C>A ENSP00000458139.1:n.*1185C>A
ENST00000566612.5:c.*759C>A ENSP00000454782.1:n.*759C>A
ENST00000611625.4:c.2582C>A ENSP00000481063.1:p.Ser861Tyr
ENST00000612417.4:c.1854-822C>A ENSP00000478360.1:n.1854-822C>A
ENST00000621016.4:c.1866-834C>A ENSP00000480664.1:n.1866-834C>A
NM_004360.3:c.2519C>A , LRG_301t1:c.2519C>A NP_004351.1:p.Ser840Tyr
XM_011523488.1:c.1784C>A XP_011521790.1:p.Ser595Tyr
XM_011523489.1:c.1784C>A XP_011521791.1:p.Ser595Tyr
NM_001317184.1:c.2336C>A NP_001304113.1:p.Ser779Tyr
NM_001317185.1:c.971C>A NP_001304114.1:p.Ser324Tyr
NM_001317186.1:c.554C>A NP_001304115.1:p.Ser185Tyr
NM_004360.4:c.2519C>A NP_004351.1:p.Ser840Tyr
NM_004360.5:c.2519C>A MANE Select NP_004351.1:p.Ser840Tyr
NM_001317184.2:c.2336C>A NP_001304113.1:p.Ser779Tyr
NM_001317185.2:c.971C>A NP_001304114.1:p.Ser324Tyr
NM_001317186.2:c.554C>A NP_001304115.1:p.Ser185Tyr
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