Canonical Allele Identifier: CA396465126
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819341T>A , CM000678.2:g.68819341T>A GRCh38
NC_000016.9:g.68853244T>A , CM000678.1:g.68853244T>A GRCh37
NC_000016.8:g.67410745T>A NCBI36
NG_008021.1:g.87050T>A , LRG_301:g.87050T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1627T>A MANE Select ENSP00000261769.4:p.Ser543Thr
ENST00000261769.9:c.1627T>A ENSP00000261769.4:p.Ser543Thr
ENST00000422392.6:c.1444T>A ENSP00000414946.2:p.Ser482Thr
ENST00000562836.5:n.1698T>A
ENST00000566510.5:c.*293T>A ENSP00000458139.1:n.*293T>A
ENST00000566612.5:c.1566-2660T>A ENSP00000454782.1:n.1566-2660T>A
ENST00000611625.4:c.1690T>A ENSP00000481063.1:p.Ser564Thr
ENST00000612417.4:c.1627T>A ENSP00000478360.1:p.Ser543Thr
ENST00000621016.4:c.1627T>A ENSP00000480664.1:p.Ser543Thr
NM_004360.3:c.1627T>A , LRG_301t1:c.1627T>A NP_004351.1:p.Ser543Thr
XM_011523488.1:c.892T>A XP_011521790.1:p.Ser298Thr
XM_011523489.1:c.892T>A XP_011521791.1:p.Ser298Thr
NM_001317184.1:c.1444T>A NP_001304113.1:p.Ser482Thr
NM_001317185.1:c.79T>A NP_001304114.1:p.Ser27Thr
NM_001317186.1:c.-254-2660T>A NP_001304115.1:n.-254-2660T>A
NM_004360.4:c.1627T>A NP_004351.1:p.Ser543Thr
NM_004360.5:c.1627T>A MANE Select NP_004351.1:p.Ser543Thr
NM_001317184.2:c.1444T>A NP_001304113.1:p.Ser482Thr
NM_001317185.2:c.79T>A NP_001304114.1:p.Ser27Thr
NM_001317186.2:c.-254-2660T>A NP_001304115.1:n.-254-2660T>A