Canonical Allele Identifier: CA10648760

Gene: CDH3

Linked Data

• ClinVar Variation Id: 320208
• ClinVar RCV Id: RCV000403396
• dbSNP Id: rs886052223
• gnomAD v2: 16-68678648-AAAAAAAG-A
• gnomAD v3: 16-68644745-AAAAAAAG-A
• gnomAD v4: 16-68644745-AAAAAAAG-A
• MyVariant Identifiers: chr16:g.68678657_68678663del (hg19) ; chr16:g.68678649_68678655del (hg19) ; chr16:g.68644754_68644760del (hg38) ; chr16:g.68644746_68644752del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68644754_68644760del , CM000678.2:g.68644754_68644760del	GRCh38
NC_000016.9:g.68678657_68678663del , CM000678.1:g.68678657_68678663del	GRCh37
NC_000016.8:g.67236158_67236164del	NCBI36
NG_009096.1:g.5507_5513del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565453.1:n.223-255_223-249del
NM_001793.4:c.-626_-620del	NP_001784.2:n.-626_-620del