Canonical Allele Identifier: CA396451483

Gene: CDH3

Linked Data

• MyVariant Identifiers: chr16:g.68714869A>G (hg19) ; chr16:g.68680966A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68680966A>G , CM000678.2:g.68680966A>G	GRCh38
NC_000016.9:g.68714869A>G , CM000678.1:g.68714869A>G	GRCh37
NC_000016.8:g.67272370A>G	NCBI36
NG_009096.1:g.41719A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264012.9:c.868-2A>G MANE Select	ENSP00000264012.4:n.868-2A>G
ENST00000264012.8:c.868-2A>G	ENSP00000264012.4:n.868-2A>G
ENST00000429102.6:c.868-2A>G	ENSP00000398485.2:n.868-2A>G
ENST00000542274.5:c.*606-2A>G	ENSP00000464021.1:n.*606-2A>G
ENST00000569036.2:c.344-2A>G
NM_001793.4:c.868-2A>G	NP_001784.2:n.868-2A>G
XM_011522800.1:c.868-2A>G	XP_011521102.1:n.868-2A>G
NM_001317195.1:c.868-2A>G	NP_001304124.1:n.868-2A>G
NM_001317196.1:c.703-2A>G	NP_001304125.1:n.703-2A>G
NM_001793.5:c.868-2A>G	NP_001784.2:n.868-2A>G
XM_011522800.3:c.868-2A>G	XP_011521102.1:n.868-2A>G
NM_001793.6:c.868-2A>G MANE Select	NP_001784.2:n.868-2A>G
NM_001317195.2:c.868-2A>G	NP_001304124.1:n.868-2A>G
NM_001317196.2:c.703-2A>G	NP_001304125.1:n.703-2A>G
NM_001317195.3:c.868-2A>G	NP_001304124.1:n.868-2A>G