Canonical Allele Identifier: CA377158464
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71798558A>G , CM000672.2:g.71798558A>G GRCh38
NC_000010.10:g.73558315A>G , CM000672.1:g.73558315A>G GRCh37
NC_000010.9:g.73228321A>G NCBI36
NG_008835.1:g.406612A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.7034A>G MANE Select ENSP00000224721.9:p.Gln2345Arg
ENST00000642965.1:c.967A>G ENSP00000495222.1:n.967A>G
ENST00000647092.1:c.631A>G ENSP00000495176.1:n.631A>G
ENST00000224721.10:c.7049A>G ENSP00000224721.8:p.Gln2350Arg
ENST00000398788.4:c.314A>G ENSP00000381768.3:p.Gln105Arg
ENST00000475158.1:n.570A>G
ENST00000619887.4:c.314A>G ENSP00000478374.1:p.Gln105Arg
ENST00000622827.4:c.7034A>G ENSP00000483211.1:p.Gln2345Arg
NM_001171933.1:c.314A>G NP_001165404.1:p.Gln105Arg
NM_001171934.1:c.314A>G NP_001165405.1:p.Gln105Arg
NM_022124.5:c.7034A>G NP_071407.4:p.Gln2345Arg
XM_006717940.2:c.7229A>G XP_006718003.1:p.Gln2410Arg
XM_006717942.2:c.7163A>G XP_006718005.1:p.Gln2388Arg
XM_011540039.1:c.7226A>G XP_011538341.1:p.Gln2409Arg
XM_011540040.1:c.7223A>G XP_011538342.1:p.Gln2408Arg
XM_011540041.1:c.7169A>G XP_011538343.1:p.Gln2390Arg
XM_011540042.1:c.7139A>G XP_011538344.1:p.Gln2380Arg
XM_011540043.1:c.7229A>G XP_011538345.1:p.Gln2410Arg
XM_011540044.1:c.7094A>G XP_011538346.1:p.Gln2365Arg
XM_011540045.1:c.7229A>G XP_011538347.1:p.Gln2410Arg
XM_011540046.1:c.6689A>G XP_011538348.1:p.Gln2230Arg
XM_011540047.1:c.6047A>G XP_011538349.1:p.Gln2016Arg
XM_011540052.1:c.3557A>G XP_011538354.1:p.Gln1186Arg
NM_022124.6:c.7034A>G MANE Select NP_071407.4:p.Gln2345Arg