Canonical Allele Identifier: CA396472081
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68867233A>C (hg19) chr16:g.68833330A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833330A>C , CM000678.2:g.68833330A>C GRCh38
NC_000016.9:g.68867233A>C , CM000678.1:g.68867233A>C GRCh37
NC_000016.8:g.67424734A>C NCBI36
NG_008021.1:g.101039A>C , LRG_301:g.101039A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2480A>C MANE Select ENSP00000261769.4:p.Tyr827Ser
ENST00000261769.9:c.2480A>C ENSP00000261769.4:p.Tyr827Ser
ENST00000422392.6:c.2297A>C ENSP00000414946.2:p.Tyr766Ser
ENST00000562118.1:n.698A>C
ENST00000562836.5:n.2551A>C
ENST00000566510.5:c.*1146A>C ENSP00000458139.1:n.*1146A>C
ENST00000566612.5:c.*720A>C ENSP00000454782.1:n.*720A>C
ENST00000611625.4:c.2543A>C ENSP00000481063.1:p.Tyr848Ser
ENST00000612417.4:c.1854-861A>C ENSP00000478360.1:n.1854-861A>C
ENST00000621016.4:c.1866-873A>C ENSP00000480664.1:n.1866-873A>C
NM_004360.3:c.2480A>C , LRG_301t1:c.2480A>C NP_004351.1:p.Tyr827Ser
XM_011523488.1:c.1745A>C XP_011521790.1:p.Tyr582Ser
XM_011523489.1:c.1745A>C XP_011521791.1:p.Tyr582Ser
NM_001317184.1:c.2297A>C NP_001304113.1:p.Tyr766Ser
NM_001317185.1:c.932A>C NP_001304114.1:p.Tyr311Ser
NM_001317186.1:c.515A>C NP_001304115.1:p.Tyr172Ser
NM_004360.4:c.2480A>C NP_004351.1:p.Tyr827Ser
NM_004360.5:c.2480A>C MANE Select NP_004351.1:p.Tyr827Ser
NM_001317184.2:c.2297A>C NP_001304113.1:p.Tyr766Ser
NM_001317185.2:c.932A>C NP_001304114.1:p.Tyr311Ser
NM_001317186.2:c.515A>C NP_001304115.1:p.Tyr172Ser
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