Canonical Allele Identifier: CA594706063
Gene: CDH23 HGNC NCBI

Linked Data

dbSNP Id: rs1378801110

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71784770_71784775del , CM000672.2:g.71784770_71784775del GRCh38
NC_000010.10:g.73544527_73544532del , CM000672.1:g.73544527_73544532del GRCh37
NC_000010.9:g.73214533_73214538del NCBI36
NG_008835.1:g.392824_392829del

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.5503-121_5503-116del MANE Select ENSP00000224721.9:n.5503-121_5503-116del
ENST00000224721.10:c.5518-121_5518-116del ENSP00000224721.8:n.5518-121_5518-116del
ENST00000622827.4:c.5503-121_5503-116del ENSP00000483211.1:n.5503-121_5503-116del
NM_022124.5:c.5503-121_5503-116del NP_071407.4:n.5503-121_5503-116del
XM_006717940.2:c.5698-121_5698-116del XP_006718003.1:n.5698-121_5698-116del
XM_006717942.2:c.5632-121_5632-116del XP_006718005.1:n.5632-121_5632-116del
XM_011540039.1:c.5695-121_5695-116del XP_011538341.1:n.5695-121_5695-116del
XM_011540040.1:c.5692-121_5692-116del XP_011538342.1:n.5692-121_5692-116del
XM_011540041.1:c.5638-121_5638-116del XP_011538343.1:n.5638-121_5638-116del
XM_011540042.1:c.5698-121_5698-116del XP_011538344.1:n.5698-121_5698-116del
XM_011540043.1:c.5698-121_5698-116del XP_011538345.1:n.5698-121_5698-116del
XM_011540044.1:c.5563-121_5563-116del XP_011538346.1:n.5563-121_5563-116del
XM_011540045.1:c.5698-121_5698-116del XP_011538347.1:n.5698-121_5698-116del
XM_011540046.1:c.5158-121_5158-116del XP_011538348.1:n.5158-121_5158-116del
XM_011540047.1:c.4516-121_4516-116del XP_011538349.1:n.4516-121_4516-116del
XM_011540048.1:c.5698-121_5698-116del XP_011538350.1:n.5698-121_5698-116del
XM_011540049.1:c.5698-121_5698-116del XP_011538351.1:n.5698-121_5698-116del
XM_011540050.1:c.5698-121_5698-116del XP_011538352.1:n.5698-121_5698-116del
XM_011540051.1:c.5698-121_5698-116del XP_011538353.1:n.5698-121_5698-116del
XM_011540052.1:c.2026-121_2026-116del XP_011538354.1:n.2026-121_2026-116del
XM_011540053.1:c.5698-121_5698-116del XP_011538355.1:n.5698-121_5698-116del
XR_945796.1:n.5941-121_5941-116del
NM_022124.6:c.5503-121_5503-116del MANE Select NP_071407.4:n.5503-121_5503-116del