Canonical Allele Identifier: CA396472441
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs765978401

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833407T>G , CM000678.2:g.68833407T>G GRCh38
NC_000016.9:g.68867310T>G , CM000678.1:g.68867310T>G GRCh37
NC_000016.8:g.67424811T>G NCBI36
NG_008021.1:g.101116T>G , LRG_301:g.101116T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2557T>G MANE Select ENSP00000261769.4:p.Ser853Ala
ENST00000261769.9:c.2557T>G ENSP00000261769.4:p.Ser853Ala
ENST00000422392.6:c.2374T>G ENSP00000414946.2:p.Ser792Ala
ENST00000562118.1:n.775T>G
ENST00000562836.5:n.2628T>G
ENST00000566510.5:c.*1223T>G ENSP00000458139.1:n.*1223T>G
ENST00000566612.5:c.*797T>G ENSP00000454782.1:n.*797T>G
ENST00000611625.4:c.2620T>G ENSP00000481063.1:p.Ser874Ala
ENST00000612417.4:c.1854-784T>G ENSP00000478360.1:n.1854-784T>G
ENST00000621016.4:c.1866-796T>G ENSP00000480664.1:n.1866-796T>G
NM_004360.3:c.2557T>G , LRG_301t1:c.2557T>G NP_004351.1:p.Ser853Ala
XM_011523488.1:c.1822T>G XP_011521790.1:p.Ser608Ala
XM_011523489.1:c.1822T>G XP_011521791.1:p.Ser608Ala
NM_001317184.1:c.2374T>G NP_001304113.1:p.Ser792Ala
NM_001317185.1:c.1009T>G NP_001304114.1:p.Ser337Ala
NM_001317186.1:c.592T>G NP_001304115.1:p.Ser198Ala
NM_004360.4:c.2557T>G NP_004351.1:p.Ser853Ala
NM_004360.5:c.2557T>G MANE Select NP_004351.1:p.Ser853Ala
NM_001317184.2:c.2374T>G NP_001304113.1:p.Ser792Ala
NM_001317185.2:c.1009T>G NP_001304114.1:p.Ser337Ala
NM_001317186.2:c.592T>G NP_001304115.1:p.Ser198Ala