Canonical Allele Identifier: CA496157476
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152142393
MyVariant Identifiers: chr16:g.68863652T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829749T>C , CM000678.2:g.68829749T>C GRCh38
NC_000016.9:g.68863652T>C , CM000678.1:g.68863652T>C GRCh37
NC_000016.8:g.67421153T>C NCBI36
NG_008021.1:g.97458T>C , LRG_301:g.97458T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2391T>C MANE Select ENSP00000261769.4:p.Tyr797=
ENST00000261769.9:c.2391T>C ENSP00000261769.4:p.Tyr797=
ENST00000422392.6:c.2208T>C ENSP00000414946.2:p.Tyr736=
ENST00000562118.1:n.609T>C
ENST00000562836.5:n.2462T>C
ENST00000566510.5:c.*1057T>C ENSP00000458139.1:n.*1057T>C
ENST00000566612.5:c.*631T>C ENSP00000454782.1:n.*631T>C
ENST00000611625.4:c.2454T>C ENSP00000481063.1:p.Tyr818=
ENST00000612417.4:c.1853+3195T>C ENSP00000478360.1:n.1853+3195T>C
ENST00000621016.4:c.1866-4454T>C ENSP00000480664.1:n.1866-4454T>C
NM_004360.3:c.2391T>C , LRG_301t1:c.2391T>C NP_004351.1:p.Tyr797=
XM_011523488.1:c.1656T>C XP_011521790.1:p.Tyr552=
XM_011523489.1:c.1656T>C XP_011521791.1:p.Tyr552=
NM_001317184.1:c.2208T>C NP_001304113.1:p.Tyr736=
NM_001317185.1:c.843T>C NP_001304114.1:p.Tyr281=
NM_001317186.1:c.426T>C NP_001304115.1:p.Tyr142=
NM_004360.4:c.2391T>C NP_004351.1:p.Tyr797=
NM_004360.5:c.2391T>C MANE Select NP_004351.1:p.Tyr797=
NM_001317184.2:c.2208T>C NP_001304113.1:p.Tyr736=
NM_001317185.2:c.843T>C NP_001304114.1:p.Tyr281=
NM_001317186.2:c.426T>C NP_001304115.1:p.Tyr142=
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