Canonical Allele Identifier: CA396471081
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1596972607

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829726A>C , CM000678.2:g.68829726A>C GRCh38
NC_000016.9:g.68863629A>C , CM000678.1:g.68863629A>C GRCh37
NC_000016.8:g.67421130A>C NCBI36
NG_008021.1:g.97435A>C , LRG_301:g.97435A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2368A>C MANE Select ENSP00000261769.4:p.Thr790Pro
ENST00000261769.9:c.2368A>C ENSP00000261769.4:p.Thr790Pro
ENST00000422392.6:c.2185A>C ENSP00000414946.2:p.Thr729Pro
ENST00000562118.1:n.586A>C
ENST00000562836.5:n.2439A>C
ENST00000566510.5:c.*1034A>C ENSP00000458139.1:n.*1034A>C
ENST00000566612.5:c.*608A>C ENSP00000454782.1:n.*608A>C
ENST00000611625.4:c.2431A>C ENSP00000481063.1:p.Thr811Pro
ENST00000612417.4:c.1853+3172A>C ENSP00000478360.1:n.1853+3172A>C
ENST00000621016.4:c.1866-4477A>C ENSP00000480664.1:n.1866-4477A>C
NM_004360.3:c.2368A>C , LRG_301t1:c.2368A>C NP_004351.1:p.Thr790Pro
XM_011523488.1:c.1633A>C XP_011521790.1:p.Thr545Pro
XM_011523489.1:c.1633A>C XP_011521791.1:p.Thr545Pro
NM_001317184.1:c.2185A>C NP_001304113.1:p.Thr729Pro
NM_001317185.1:c.820A>C NP_001304114.1:p.Thr274Pro
NM_001317186.1:c.403A>C NP_001304115.1:p.Thr135Pro
NM_004360.4:c.2368A>C NP_004351.1:p.Thr790Pro
NM_004360.5:c.2368A>C MANE Select NP_004351.1:p.Thr790Pro
NM_001317184.2:c.2185A>C NP_001304113.1:p.Thr729Pro
NM_001317185.2:c.820A>C NP_001304114.1:p.Thr274Pro
NM_001317186.2:c.403A>C NP_001304115.1:p.Thr135Pro