Canonical Allele Identifier: CA8128887

Gene: CDH3

Linked Data

• ClinVar Variation Id: 320221
• ClinVar RCV Id: RCV000346627
• dbSNP Id: rs373351410
• ExAC: 16:68679247 C / T
• gnomAD v2: 16-68679247-C-T
• gnomAD v3: 16-68645344-C-T
• gnomAD v4: 16-68645344-C-T
• MyVariant Identifiers: chr16:g.68679247C>T (hg19) ; chr16:g.68645344C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68645344C>T , CM000678.2:g.68645344C>T	GRCh38
NC_000016.9:g.68679247C>T , CM000678.1:g.68679247C>T	GRCh37
NC_000016.8:g.67236748C>T	NCBI36
NG_009096.1:g.6097C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264012.9:c.-36C>T MANE Select	ENSP00000264012.4:n.-36C>T
ENST00000264012.8:c.-36C>T	ENSP00000264012.4:n.-36C>T
ENST00000429102.6:c.-36C>T	ENSP00000398485.2:n.-36C>T
ENST00000542274.5:c.-36C>T	ENSP00000464021.1:n.-36C>T
NM_001793.4:c.-36C>T	NP_001784.2:n.-36C>T
XM_011522800.1:c.-36C>T	XP_011521102.1:n.-36C>T
NM_001317195.1:c.-36C>T	NP_001304124.1:n.-36C>T
NM_001317196.1:c.-86C>T	NP_001304125.1:n.-86C>T
NM_001793.5:c.-36C>T	NP_001784.2:n.-36C>T
XM_011522800.3:c.-36C>T	XP_011521102.1:n.-36C>T
NM_001793.6:c.-36C>T MANE Select	NP_001784.2:n.-36C>T
NM_001317195.2:c.-36C>T	NP_001304124.1:n.-36C>T
NM_001317196.2:c.-86C>T	NP_001304125.1:n.-86C>T
NM_001317195.3:c.-36C>T	NP_001304124.1:n.-36C>T