Canonical Allele Identifier: CA396472536
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 963573
ClinVar RCV Id: RCV001237616
dbSNP Id: rs765545887
MyVariant Identifiers: chr16:g.68867330T>A (hg19) chr16:g.68833427T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833427T>A , CM000678.2:g.68833427T>A GRCh38
NC_000016.9:g.68867330T>A , CM000678.1:g.68867330T>A GRCh37
NC_000016.8:g.67424831T>A NCBI36
NG_008021.1:g.101136T>A , LRG_301:g.101136T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2577T>A MANE Select ENSP00000261769.4:p.Tyr859Ter
ENST00000261769.9:c.2577T>A ENSP00000261769.4:p.Tyr859Ter
ENST00000422392.6:c.2394T>A ENSP00000414946.2:p.Tyr798Ter
ENST00000562118.1:n.795T>A
ENST00000562836.5:n.2648T>A
ENST00000566510.5:c.*1243T>A ENSP00000458139.1:n.*1243T>A
ENST00000566612.5:c.*817T>A ENSP00000454782.1:n.*817T>A
ENST00000611625.4:c.2640T>A ENSP00000481063.1:p.Tyr880Ter
ENST00000612417.4:c.1854-764T>A ENSP00000478360.1:n.1854-764T>A
ENST00000621016.4:c.1866-776T>A ENSP00000480664.1:n.1866-776T>A
NM_004360.3:c.2577T>A , LRG_301t1:c.2577T>A NP_004351.1:p.Tyr859Ter
XM_011523488.1:c.1842T>A XP_011521790.1:p.Tyr614Ter
XM_011523489.1:c.1842T>A XP_011521791.1:p.Tyr614Ter
NM_001317184.1:c.2394T>A NP_001304113.1:p.Tyr798Ter
NM_001317185.1:c.1029T>A NP_001304114.1:p.Tyr343Ter
NM_001317186.1:c.612T>A NP_001304115.1:p.Tyr204Ter
NM_004360.4:c.2577T>A NP_004351.1:p.Tyr859Ter
NM_004360.5:c.2577T>A MANE Select NP_004351.1:p.Tyr859Ter
NM_001317184.2:c.2394T>A NP_001304113.1:p.Tyr798Ter
NM_001317185.2:c.1029T>A NP_001304114.1:p.Tyr343Ter
NM_001317186.2:c.612T>A NP_001304115.1:p.Tyr204Ter
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