Canonical Allele Identifier: CA396451532

Gene: CDH3

Linked Data

• gnomAD v4: 16-68680975-C-T
• MyVariant Identifiers: chr16:g.68714878C>T (hg19) ; chr16:g.68680975C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68680975C>T , CM000678.2:g.68680975C>T	GRCh38
NC_000016.9:g.68714878C>T , CM000678.1:g.68714878C>T	GRCh37
NC_000016.8:g.67272379C>T	NCBI36
NG_009096.1:g.41728C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264012.9:c.875C>T MANE Select	ENSP00000264012.4:p.Pro292Leu
ENST00000264012.8:c.875C>T	ENSP00000264012.4:p.Pro292Leu
ENST00000429102.6:c.875C>T	ENSP00000398485.2:p.Pro292Leu
ENST00000542274.5:c.*613C>T	ENSP00000464021.1:n.*613C>T
ENST00000569036.2:c.351C>T
NM_001793.4:c.875C>T	NP_001784.2:p.Pro292Leu
XM_011522800.1:c.875C>T	XP_011521102.1:p.Pro292Leu
NM_001317195.1:c.875C>T	NP_001304124.1:p.Pro292Leu
NM_001317196.1:c.710C>T	NP_001304125.1:p.Pro237Leu
NM_001793.5:c.875C>T	NP_001784.2:p.Pro292Leu
XM_011522800.3:c.875C>T	XP_011521102.1:p.Pro292Leu
NM_001793.6:c.875C>T MANE Select	NP_001784.2:p.Pro292Leu
NM_001317195.2:c.875C>T	NP_001304124.1:p.Pro292Leu
NM_001317196.2:c.710C>T	NP_001304125.1:p.Pro237Leu
NM_001317195.3:c.875C>T	NP_001304124.1:p.Pro292Leu