Canonical Allele Identifier: CA496153980

Gene: CDH3

Linked Data

• gnomAD v4: 16-68680976-T-G
• MyVariant Identifiers: chr16:g.68714879T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68680976T>G , CM000678.2:g.68680976T>G	GRCh38
NC_000016.9:g.68714879T>G , CM000678.1:g.68714879T>G	GRCh37
NC_000016.8:g.67272380T>G	NCBI36
NG_009096.1:g.41729T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264012.9:c.876T>G MANE Select	ENSP00000264012.4:p.Pro292=
ENST00000264012.8:c.876T>G	ENSP00000264012.4:p.Pro292=
ENST00000429102.6:c.876T>G	ENSP00000398485.2:p.Pro292=
ENST00000542274.5:c.*614T>G	ENSP00000464021.1:n.*614T>G
ENST00000569036.2:c.352T>G
NM_001793.4:c.876T>G	NP_001784.2:p.Pro292=
XM_011522800.1:c.876T>G	XP_011521102.1:p.Pro292=
NM_001317195.1:c.876T>G	NP_001304124.1:p.Pro292=
NM_001317196.1:c.711T>G	NP_001304125.1:p.Pro237=
NM_001793.5:c.876T>G	NP_001784.2:p.Pro292=
XM_011522800.3:c.876T>G	XP_011521102.1:p.Pro292=
NM_001793.6:c.876T>G MANE Select	NP_001784.2:p.Pro292=
NM_001317195.2:c.876T>G	NP_001304124.1:p.Pro292=
NM_001317196.2:c.711T>G	NP_001304125.1:p.Pro237=
NM_001317195.3:c.876T>G	NP_001304124.1:p.Pro292=