Canonical Allele Identifier: CA8129091

Gene: CDH3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68678876C>T , CM000678.2:g.68678876C>T	GRCh38
NC_000016.9:g.68712779C>T , CM000678.1:g.68712779C>T	GRCh37
NC_000016.8:g.67270280C>T	NCBI36
NG_009096.1:g.39629C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001793.6:c.661C>T MANE Select	NP_001784.2:p.Arg221Ter
ENST00000264012.9:c.661C>T MANE Select	ENSP00000264012.4:p.Arg221Ter
NM_001317195.1:c.661C>T	NP_001304124.1:p.Arg221Ter
NM_001317195.2:c.661C>T	NP_001304124.1:p.Arg221Ter
NM_001317195.3:c.661C>T	NP_001304124.1:p.Arg221Ter
NM_001317196.1:c.496C>T	NP_001304125.1:p.Arg166Ter
NM_001317196.2:c.496C>T	NP_001304125.1:p.Arg166Ter
NM_001793.4:c.661C>T	NP_001784.2:p.Arg221Ter
NM_001793.5:c.661C>T	NP_001784.2:p.Arg221Ter
ENST00000264012.8:c.661C>T	ENSP00000264012.4:p.Arg221Ter
ENST00000429102.6:c.661C>T	ENSP00000398485.2:p.Arg221Ter
ENST00000542274.5:c.*399C>T	ENSP00000464021.1:n.*399C>T
ENST00000566808.2:c.529C>T
ENST00000569036.2:c.167+220C>T
XM_011522800.1:c.661C>T	XP_011521102.1:p.Arg221Ter
XM_011522800.3:c.661C>T	XP_011521102.1:p.Arg221Ter