Canonical Allele Identifier: CA8129839
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 463778
ClinVar RCV Id: RCV000535540
dbSNP Id: rs746703615

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801883C>A , CM000678.2:g.68801883C>A GRCh38
NC_000016.9:g.68835786C>A , CM000678.1:g.68835786C>A GRCh37
NC_000016.8:g.67393287C>A NCBI36
NG_008021.1:g.69592C>A , LRG_301:g.69592C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.377C>A MANE Select ENSP00000261769.4:p.Pro126Gln
ENST00000261769.9:c.377C>A ENSP00000261769.4:p.Pro126Gln
ENST00000422392.6:c.377C>A ENSP00000414946.2:p.Pro126Gln
ENST00000561751.1:n.144C>A
ENST00000562836.5:n.448C>A
ENST00000564676.5:n.659C>A
ENST00000564745.1:n.372C>A
ENST00000566510.5:c.377C>A ENSP00000458139.1:p.Pro126Gln
ENST00000566612.5:c.377C>A ENSP00000454782.1:p.Pro126Gln
ENST00000611625.4:c.377C>A ENSP00000481063.1:p.Pro126Gln
ENST00000612417.4:c.377C>A ENSP00000478360.1:p.Pro126Gln
ENST00000621016.4:c.377C>A ENSP00000480664.1:p.Pro126Gln
NM_004360.3:c.377C>A , LRG_301t1:c.377C>A NP_004351.1:p.Pro126Gln
XM_011523488.1:c.-359C>A XP_011521790.1:p.=
XM_011523489.1:c.-359C>A XP_011521791.1:p.=
NM_001317184.1:c.377C>A NP_001304113.1:p.Pro126Gln
NM_001317185.1:c.-1239C>A NP_001304114.1:p.=
NM_001317186.1:c.-1443C>A NP_001304115.1:p.=
NM_004360.4:c.377C>A NP_004351.1:p.Pro126Gln
NM_004360.5:c.377C>A MANE Select NP_004351.1:p.Pro126Gln
NM_001317184.2:c.377C>A NP_001304113.1:p.Pro126Gln
NM_001317185.2:c.-1239C>A NP_001304114.1:p.=
NM_001317186.2:c.-1443C>A NP_001304115.1:p.=