Canonical Allele Identifier: CA168064
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142321
dbSNP Id: rs587782381

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819399C>G , CM000678.2:g.68819399C>G GRCh38
NC_000016.9:g.68853302C>G , CM000678.1:g.68853302C>G GRCh37
NC_000016.8:g.67410803C>G NCBI36
NG_008021.1:g.87108C>G , LRG_301:g.87108C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1685C>G MANE Select ENSP00000261769.4:p.Thr562Arg
ENST00000261769.9:c.1685C>G ENSP00000261769.4:p.Thr562Arg
ENST00000422392.6:c.1502C>G ENSP00000414946.2:p.Thr501Arg
ENST00000562836.5:n.1756C>G
ENST00000566510.5:c.*351C>G ENSP00000458139.1:p.=
ENST00000566612.5:c.1566-2602C>G ENSP00000454782.1:p.=
ENST00000611625.4:c.1748C>G ENSP00000481063.1:p.Thr583Arg
ENST00000612417.4:c.1685C>G ENSP00000478360.1:p.Thr562Arg
ENST00000621016.4:c.1685C>G ENSP00000480664.1:p.Thr562Arg
NM_004360.3:c.1685C>G , LRG_301t1:c.1685C>G NP_004351.1:p.Thr562Arg
XM_011523488.1:c.950C>G XP_011521790.1:p.Thr317Arg
XM_011523489.1:c.950C>G XP_011521791.1:p.Thr317Arg
NM_001317184.1:c.1502C>G NP_001304113.1:p.Thr501Arg
NM_001317185.1:c.137C>G NP_001304114.1:p.Thr46Arg
NM_001317186.1:c.-254-2602C>G NP_001304115.1:p.=
NM_004360.4:c.1685C>G NP_004351.1:p.Thr562Arg
NM_004360.5:c.1685C>G MANE Select NP_004351.1:p.Thr562Arg
NM_001317184.2:c.1502C>G NP_001304113.1:p.Thr501Arg
NM_001317185.2:c.137C>G NP_001304114.1:p.Thr46Arg
NM_001317186.2:c.-254-2602C>G NP_001304115.1:p.=