Canonical Allele Identifier: CA496148823
Gene: CDH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1973140
ClinVar RCV Id: RCV002731050
dbSNP Id: rs992399939

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68645668G>C , CM000678.2:g.68645668G>C GRCh38
NC_000016.9:g.68679571G>C , CM000678.1:g.68679571G>C GRCh37
NC_000016.8:g.67237072G>C NCBI36
NG_009096.1:g.6421G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264012.9:c.78G>C MANE Select ENSP00000264012.4:p.Pro26=
ENST00000264012.8:c.78G>C ENSP00000264012.4:p.Pro26=
ENST00000429102.6:c.78G>C ENSP00000398485.2:p.Pro26=
ENST00000542274.5:c.45+244G>C ENSP00000464021.1:n.45+244G>C
ENST00000566808.2:c.32G>C
NM_001793.4:c.78G>C NP_001784.2:p.Pro26=
XM_011522800.1:c.78G>C XP_011521102.1:p.Pro26=
NM_001317195.1:c.78G>C NP_001304124.1:p.Pro26=
NM_001317196.1:c.-6+244G>C NP_001304125.1:n.-6+244G>C
NM_001793.5:c.78G>C NP_001784.2:p.Pro26=
XM_011522800.3:c.78G>C XP_011521102.1:p.Pro26=
NM_001793.6:c.78G>C MANE Select NP_001784.2:p.Pro26=
NM_001317195.2:c.78G>C NP_001304124.1:p.Pro26=
NM_001317196.2:c.-6+244G>C NP_001304125.1:n.-6+244G>C
NM_001317195.3:c.78G>C NP_001304124.1:p.Pro26=