Canonical Allele Identifier: CA496153976
Gene: CDH3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68714873A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68680970A>G , CM000678.2:g.68680970A>G GRCh38
NC_000016.9:g.68714873A>G , CM000678.1:g.68714873A>G GRCh37
NC_000016.8:g.67272374A>G NCBI36
NG_009096.1:g.41723A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264012.9:c.870A>G MANE Select ENSP00000264012.4:p.Lys290=
ENST00000264012.8:c.870A>G ENSP00000264012.4:p.Lys290=
ENST00000429102.6:c.870A>G ENSP00000398485.2:p.Lys290=
ENST00000542274.5:c.*608A>G ENSP00000464021.1:n.*608A>G
ENST00000569036.2:c.346A>G
NM_001793.4:c.870A>G NP_001784.2:p.Lys290=
XM_011522800.1:c.870A>G XP_011521102.1:p.Lys290=
NM_001317195.1:c.870A>G NP_001304124.1:p.Lys290=
NM_001317196.1:c.705A>G NP_001304125.1:p.Lys235=
NM_001793.5:c.870A>G NP_001784.2:p.Lys290=
XM_011522800.3:c.870A>G XP_011521102.1:p.Lys290=
NM_001793.6:c.870A>G MANE Select NP_001784.2:p.Lys290=
NM_001317195.2:c.870A>G NP_001304124.1:p.Lys290=
NM_001317196.2:c.705A>G NP_001304125.1:p.Lys235=
NM_001317195.3:c.870A>G NP_001304124.1:p.Lys290=