Canonical Allele Identifier: CA915945951

Gene: CDH23

Linked Data

• ClinVar Variation Id: 636159
• ClinVar RCV Id: RCV000787805
• dbSNP Id: rs1589420011

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785098_71785103del , CM000672.2:g.71785098_71785103del	GRCh38
NC_000010.10:g.73544855_73544860del , CM000672.1:g.73544855_73544860del	GRCh37
NC_000010.9:g.73214861_73214866del	NCBI36
NG_008835.1:g.393152_393157del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5710_5712+3del
ENST00000224721.10:c.5725_5727+3del
ENST00000622827.4:c.5710_5712+3del
NM_022124.5:c.5710_5712+3del
XM_006717940.2:c.5905_5907+3del
XM_006717942.2:c.5839_5841+3del
XM_011540039.1:c.5902_5904+3del
XM_011540040.1:c.5899_5901+3del
XM_011540041.1:c.5845_5847+3del
XM_011540042.1:c.5905_5907+3del
XM_011540043.1:c.5905_5907+3del
XM_011540044.1:c.5770_5772+3del
XM_011540045.1:c.5905_5907+3del
XM_011540046.1:c.5365_5367+3del
XM_011540047.1:c.4723_4725+3del
XM_011540048.1:c.5905_5907+3del
XM_011540049.1:c.5905_5907+3del
XM_011540050.1:c.5905_5907+3del
XM_011540051.1:c.5905_5907+3del
XM_011540052.1:c.2233_2235+3del
XM_011540053.1:c.5905_5907+3del
XR_945796.1:n.6148_6150+3del
NM_022124.6:c.5710_5712+3del