Canonical Allele Identifier: CA396451526

Gene: CDH3

Linked Data

• MyVariant Identifiers: chr16:g.68714877C>T (hg19) ; chr16:g.68680974C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68680974C>T , CM000678.2:g.68680974C>T	GRCh38
NC_000016.9:g.68714877C>T , CM000678.1:g.68714877C>T	GRCh37
NC_000016.8:g.67272378C>T	NCBI36
NG_009096.1:g.41727C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264012.9:c.874C>T MANE Select	ENSP00000264012.4:p.Pro292Ser
ENST00000264012.8:c.874C>T	ENSP00000264012.4:p.Pro292Ser
ENST00000429102.6:c.874C>T	ENSP00000398485.2:p.Pro292Ser
ENST00000542274.5:c.*612C>T	ENSP00000464021.1:n.*612C>T
ENST00000569036.2:c.350C>T
NM_001793.4:c.874C>T	NP_001784.2:p.Pro292Ser
XM_011522800.1:c.874C>T	XP_011521102.1:p.Pro292Ser
NM_001317195.1:c.874C>T	NP_001304124.1:p.Pro292Ser
NM_001317196.1:c.709C>T	NP_001304125.1:p.Pro237Ser
NM_001793.5:c.874C>T	NP_001784.2:p.Pro292Ser
XM_011522800.3:c.874C>T	XP_011521102.1:p.Pro292Ser
NM_001793.6:c.874C>T MANE Select	NP_001784.2:p.Pro292Ser
NM_001317195.2:c.874C>T	NP_001304124.1:p.Pro292Ser
NM_001317196.2:c.709C>T	NP_001304125.1:p.Pro237Ser
NM_001317195.3:c.874C>T	NP_001304124.1:p.Pro292Ser