Canonical Allele Identifier: CA396455682

Gene: CDH3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68691842T>G , CM000678.2:g.68691842T>G	GRCh38
NC_000016.9:g.68725745T>G , CM000678.1:g.68725745T>G	GRCh37
NC_000016.8:g.67283246T>G	NCBI36
NG_009096.1:g.52595T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001793.6:c.1918T>G MANE Select	NP_001784.2:p.Cys640Gly
ENST00000264012.9:c.1918T>G MANE Select	ENSP00000264012.4:p.Cys640Gly
NM_001317195.1:c.1918T>G	NP_001304124.1:p.Cys640Gly
NM_001317195.2:c.1918T>G	NP_001304124.1:p.Cys640Gly
NM_001317195.3:c.1918T>G	NP_001304124.1:p.Cys640Gly
NM_001317196.1:c.1753T>G	NP_001304125.1:p.Cys585Gly
NM_001317196.2:c.1753T>G	NP_001304125.1:p.Cys585Gly
NM_001793.4:c.1918T>G	NP_001784.2:p.Cys640Gly
NM_001793.5:c.1918T>G	NP_001784.2:p.Cys640Gly
ENST00000264012.8:c.1918T>G	ENSP00000264012.4:p.Cys640Gly
ENST00000429102.6:c.1918T>G	ENSP00000398485.2:p.Cys640Gly
ENST00000542274.5:c.*1656T>G	ENSP00000464021.1:n.*1656T>G
ENST00000567674.1:c.248T>G
XM_011522800.1:c.1918T>G	XP_011521102.1:p.Cys640Gly
XM_011522800.3:c.1918T>G	XP_011521102.1:p.Cys640Gly