Canonical Allele Identifier: CA396453064

Gene: CDH3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68682368G>T , CM000678.2:g.68682368G>T	GRCh38
NC_000016.9:g.68716271G>T , CM000678.1:g.68716271G>T	GRCh37
NC_000016.8:g.67273772G>T	NCBI36
NG_009096.1:g.43121G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001793.6:c.1063G>T MANE Select	NP_001784.2:p.Asp355Tyr
ENST00000264012.9:c.1063G>T MANE Select	ENSP00000264012.4:p.Asp355Tyr
NM_001317195.1:c.1063G>T	NP_001304124.1:p.Asp355Tyr
NM_001317195.2:c.1063G>T	NP_001304124.1:p.Asp355Tyr
NM_001317195.3:c.1063G>T	NP_001304124.1:p.Asp355Tyr
NM_001317196.1:c.898G>T	NP_001304125.1:p.Asp300Tyr
NM_001317196.2:c.898G>T	NP_001304125.1:p.Asp300Tyr
NM_001793.4:c.1063G>T	NP_001784.2:p.Asp355Tyr
NM_001793.5:c.1063G>T	NP_001784.2:p.Asp355Tyr
ENST00000264012.8:c.1063G>T	ENSP00000264012.4:p.Asp355Tyr
ENST00000429102.6:c.1063G>T	ENSP00000398485.2:p.Asp355Tyr
ENST00000542274.5:c.*801G>T	ENSP00000464021.1:n.*801G>T
ENST00000569036.2:c.539G>T
XM_011522800.1:c.1063G>T	XP_011521102.1:p.Asp355Tyr
XM_011522800.3:c.1063G>T	XP_011521102.1:p.Asp355Tyr