Canonical Allele Identifier: CA396464872
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819295A>C , CM000678.2:g.68819295A>C GRCh38
NC_000016.9:g.68853198A>C , CM000678.1:g.68853198A>C GRCh37
NC_000016.8:g.67410699A>C NCBI36
NG_008021.1:g.87004A>C , LRG_301:g.87004A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1581A>C MANE Select ENSP00000261769.4:p.Arg527Ser
ENST00000261769.9:c.1581A>C ENSP00000261769.4:p.Arg527Ser
ENST00000422392.6:c.1398A>C ENSP00000414946.2:p.Arg466Ser
ENST00000562836.5:n.1652A>C
ENST00000566510.5:c.*247A>C ENSP00000458139.1:n.*247A>C
ENST00000566612.5:c.1566-2706A>C ENSP00000454782.1:n.1566-2706A>C
ENST00000611625.4:c.1644A>C ENSP00000481063.1:p.Arg548Ser
ENST00000612417.4:c.1581A>C ENSP00000478360.1:p.Arg527Ser
ENST00000621016.4:c.1581A>C ENSP00000480664.1:p.Arg527Ser
NM_004360.3:c.1581A>C , LRG_301t1:c.1581A>C NP_004351.1:p.Arg527Ser
XM_011523488.1:c.846A>C XP_011521790.1:p.Arg282Ser
XM_011523489.1:c.846A>C XP_011521791.1:p.Arg282Ser
NM_001317184.1:c.1398A>C NP_001304113.1:p.Arg466Ser
NM_001317185.1:c.33A>C NP_001304114.1:p.Arg11Ser
NM_001317186.1:c.-254-2706A>C NP_001304115.1:n.-254-2706A>C
NM_004360.4:c.1581A>C NP_004351.1:p.Arg527Ser
NM_004360.5:c.1581A>C MANE Select NP_004351.1:p.Arg527Ser
NM_001317184.2:c.1398A>C NP_001304113.1:p.Arg466Ser
NM_001317185.2:c.33A>C NP_001304114.1:p.Arg11Ser
NM_001317186.2:c.-254-2706A>C NP_001304115.1:n.-254-2706A>C