Canonical Allele Identifier: CA8128903
Gene: CDH3 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68645430C>A , CM000678.2:g.68645430C>A GRCh38
NC_000016.9:g.68679333C>A , CM000678.1:g.68679333C>A GRCh37
NC_000016.8:g.67236834C>A NCBI36
NG_009096.1:g.6183C>A

Transcript Alleles

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