Canonical Allele Identifier: CA2229884334
Gene: CDH3 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000264012.9:c.869A= MANE Select ENSP00000264012.4:p.Lys290=
ENST00000264012.8:c.869A= ENSP00000264012.4:p.Lys290=
ENST00000429102.6:c.869A= ENSP00000398485.2:p.Lys290=
ENST00000542274.5:c.*607A= ENSP00000464021.1:n.*607A=
ENST00000569036.2:c.345A=
NM_001793.4:c.869A= NP_001784.2:p.Lys290=
XM_011522800.1:c.869A= XP_011521102.1:p.Lys290=
NM_001317195.1:c.869A= NP_001304124.1:p.Lys290=
NM_001317196.1:c.704A= NP_001304125.1:p.Lys235=
NM_001793.5:c.869A= NP_001784.2:p.Lys290=
XM_011522800.3:c.869A= XP_011521102.1:p.Lys290=
NM_001793.6:c.869A= MANE Select NP_001784.2:p.Lys290=
NM_001317195.2:c.869A= NP_001304124.1:p.Lys290=
NM_001317196.2:c.704A= NP_001304125.1:p.Lys235=
NM_001317195.3:c.869A= NP_001304124.1:p.Lys290=