Canonical Allele Identifier: CA915945959

Gene: CDH23

Linked Data

• ClinVar Variation Id: 810981
• ClinVar RCV Id: RCV001000491 ; RCV001809886
• dbSNP Id: rs1589292855

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71645832del , CM000672.2:g.71645832del	GRCh38
NC_000010.10:g.73405589del , CM000672.1:g.73405589del	GRCh37
NC_000010.9:g.73075595del	NCBI36
NG_008835.1:g.253886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.1142del
ENST00000398809.9:c.1142del
ENST00000442677.4:c.1142del
ENST00000466757.8:c.573del
ENST00000643732.1:n.978del
ENST00000646131.1:c.806del
ENST00000224721.10:c.1157del
ENST00000299366.11:c.1142del
ENST00000398809.8:c.1142del
ENST00000398842.7:c.887del
ENST00000461841.7:c.1142del
ENST00000466757.7:c.573del
ENST00000470494.5:c.111del
ENST00000616684.4:c.1142del
ENST00000622827.4:c.1142del	ENSP00000483211.1:p.Gly381AlafsTer2
NM_001171930.1:c.1142del
NM_001171931.1:c.1142del
NM_022124.5:c.1142del
NM_052836.3:c.1142del
XM_006717940.2:c.1337del
XM_006717942.2:c.1271del
XM_011540039.1:c.1337del
XM_011540040.1:c.1331del
XM_011540041.1:c.1277del
XM_011540042.1:c.1337del
XM_011540043.1:c.1337del
XM_011540044.1:c.1202del
XM_011540045.1:c.1337del
XM_011540046.1:c.797del
XM_011540047.1:c.155del
XM_011540048.1:c.1337del
XM_011540049.1:c.1337del
XM_011540050.1:c.1337del
XM_011540051.1:c.1337del
XM_011540053.1:c.1337del
XM_011540054.1:c.1277del
XR_945796.1:n.1580del
NM_001171930.2:c.1142del
NM_001171931.2:c.1142del
NM_022124.6:c.1142del
NM_052836.4:c.1142del