Canonical Allele Identifier: CA377158461
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71798557C>G , CM000672.2:g.71798557C>G GRCh38
NC_000010.10:g.73558314C>G , CM000672.1:g.73558314C>G GRCh37
NC_000010.9:g.73228320C>G NCBI36
NG_008835.1:g.406611C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.7033C>G MANE Select ENSP00000224721.9:p.Gln2345Glu
ENST00000642965.1:c.966C>G ENSP00000495222.1:n.966C>G
ENST00000647092.1:c.630C>G ENSP00000495176.1:n.630C>G
ENST00000224721.10:c.7048C>G ENSP00000224721.8:p.Gln2350Glu
ENST00000398788.4:c.313C>G ENSP00000381768.3:p.Gln105Glu
ENST00000475158.1:n.569C>G
ENST00000619887.4:c.313C>G ENSP00000478374.1:p.Gln105Glu
ENST00000622827.4:c.7033C>G ENSP00000483211.1:p.Gln2345Glu
NM_001171933.1:c.313C>G NP_001165404.1:p.Gln105Glu
NM_001171934.1:c.313C>G NP_001165405.1:p.Gln105Glu
NM_022124.5:c.7033C>G NP_071407.4:p.Gln2345Glu
XM_006717940.2:c.7228C>G XP_006718003.1:p.Gln2410Glu
XM_006717942.2:c.7162C>G XP_006718005.1:p.Gln2388Glu
XM_011540039.1:c.7225C>G XP_011538341.1:p.Gln2409Glu
XM_011540040.1:c.7222C>G XP_011538342.1:p.Gln2408Glu
XM_011540041.1:c.7168C>G XP_011538343.1:p.Gln2390Glu
XM_011540042.1:c.7138C>G XP_011538344.1:p.Gln2380Glu
XM_011540043.1:c.7228C>G XP_011538345.1:p.Gln2410Glu
XM_011540044.1:c.7093C>G XP_011538346.1:p.Gln2365Glu
XM_011540045.1:c.7228C>G XP_011538347.1:p.Gln2410Glu
XM_011540046.1:c.6688C>G XP_011538348.1:p.Gln2230Glu
XM_011540047.1:c.6046C>G XP_011538349.1:p.Gln2016Glu
XM_011540052.1:c.3556C>G XP_011538354.1:p.Gln1186Glu
NM_022124.6:c.7033C>G MANE Select NP_071407.4:p.Gln2345Glu