Canonical Allele Identifier: CA283273982
Gene: CDH3 HGNC NCBI

Linked Data

dbSNP Id: rs1004266291

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68680969A>C , CM000678.2:g.68680969A>C GRCh38
NC_000016.9:g.68714872A>C , CM000678.1:g.68714872A>C GRCh37
NC_000016.8:g.67272373A>C NCBI36
NG_009096.1:g.41722A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264012.9:c.869A>C MANE Select ENSP00000264012.4:p.Lys290Thr
ENST00000264012.8:c.869A>C ENSP00000264012.4:p.Lys290Thr
ENST00000429102.6:c.869A>C ENSP00000398485.2:p.Lys290Thr
ENST00000542274.5:c.*607A>C ENSP00000464021.1:n.*607A>C
ENST00000569036.2:c.345A>C
NM_001793.4:c.869A>C NP_001784.2:p.Lys290Thr
XM_011522800.1:c.869A>C XP_011521102.1:p.Lys290Thr
NM_001317195.1:c.869A>C NP_001304124.1:p.Lys290Thr
NM_001317196.1:c.704A>C NP_001304125.1:p.Lys235Thr
NM_001793.5:c.869A>C NP_001784.2:p.Lys290Thr
XM_011522800.3:c.869A>C XP_011521102.1:p.Lys290Thr
NM_001793.6:c.869A>C MANE Select NP_001784.2:p.Lys290Thr
NM_001317195.2:c.869A>C NP_001304124.1:p.Lys290Thr
NM_001317196.2:c.704A>C NP_001304125.1:p.Lys235Thr
NM_001317195.3:c.869A>C NP_001304124.1:p.Lys290Thr