Canonical Allele Identifier: CA2839202980
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71785066del , CM000672.2:g.71785066del GRCh38
NC_000010.10:g.73544823del , CM000672.1:g.73544823del GRCh37
NC_000010.9:g.73214829del NCBI36
NG_008835.1:g.393120del

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.5678del MANE Select ENSP00000224721.9:p.Gly1893AlafsTer18
ENST00000224721.10:c.5693del ENSP00000224721.8:p.Gly1898AlafsTer18
ENST00000622827.4:c.5678del ENSP00000483211.1:p.Gly1893AlafsTer18
NM_022124.5:c.5678del NP_071407.4:p.Gly1893AlafsTer18
XM_006717940.2:c.5873del XP_006718003.1:p.Gly1958AlafsTer18
XM_006717942.2:c.5807del XP_006718005.1:p.Gly1936AlafsTer18
XM_011540039.1:c.5870del XP_011538341.1:p.Gly1957AlafsTer18
XM_011540040.1:c.5867del XP_011538342.1:p.Gly1956AlafsTer18
XM_011540041.1:c.5813del XP_011538343.1:p.Gly1938AlafsTer18
XM_011540042.1:c.5873del XP_011538344.1:p.Gly1958AlafsTer18
XM_011540043.1:c.5873del XP_011538345.1:p.Gly1958AlafsTer18
XM_011540044.1:c.5738del XP_011538346.1:p.Gly1913AlafsTer18
XM_011540045.1:c.5873del XP_011538347.1:p.Gly1958AlafsTer18
XM_011540046.1:c.5333del XP_011538348.1:p.Gly1778AlafsTer18
XM_011540047.1:c.4691del XP_011538349.1:p.Gly1564AlafsTer18
XM_011540048.1:c.5873del XP_011538350.1:p.Gly1958AlafsTer18
XM_011540049.1:c.5873del XP_011538351.1:p.Gly1958AlafsTer18
XM_011540050.1:c.5873del XP_011538352.1:p.Gly1958AlafsTer18
XM_011540051.1:c.5873del XP_011538353.1:p.Gly1958AlafsTer18
XM_011540052.1:c.2201del XP_011538354.1:p.Gly734AlafsTer18
XM_011540053.1:c.5873del XP_011538355.1:p.Gly1958AlafsTer18
XR_945796.1:n.6116del
NM_022124.6:c.5678del MANE Select NP_071407.4:p.Gly1893AlafsTer18