Canonical Allele Identifier: CA377131630
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71807689A>T , CM000672.2:g.71807689A>T GRCh38
NC_000010.10:g.73567446A>T , CM000672.1:g.73567446A>T GRCh37
NC_000010.9:g.73237452A>T NCBI36
NG_008835.1:g.415743A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.8482A>T MANE Select ENSP00000224721.9:p.Thr2828Ser
ENST00000642965.1:c.2415A>T ENSP00000495222.1:n.2415A>T
ENST00000647092.1:c.2079A>T ENSP00000495176.1:n.2079A>T
ENST00000224721.10:c.8497A>T ENSP00000224721.8:p.Thr2833Ser
ENST00000398788.4:c.1762A>T ENSP00000381768.3:p.Thr588Ser
ENST00000475158.1:n.2018A>T
ENST00000619887.4:c.1762A>T ENSP00000478374.1:p.Thr588Ser
ENST00000622827.4:c.8482A>T ENSP00000483211.1:p.Thr2828Ser
NM_001171933.1:c.1762A>T NP_001165404.1:p.Thr588Ser
NM_001171934.1:c.1762A>T NP_001165405.1:p.Thr588Ser
NM_022124.5:c.8482A>T NP_071407.4:p.Thr2828Ser
XM_006717940.2:c.8677A>T XP_006718003.1:p.Thr2893Ser
XM_006717942.2:c.8611A>T XP_006718005.1:p.Thr2871Ser
XM_011540039.1:c.8674A>T XP_011538341.1:p.Thr2892Ser
XM_011540040.1:c.8671A>T XP_011538342.1:p.Thr2891Ser
XM_011540041.1:c.8617A>T XP_011538343.1:p.Thr2873Ser
XM_011540042.1:c.8587A>T XP_011538344.1:p.Thr2863Ser
XM_011540043.1:c.8677A>T XP_011538345.1:p.Thr2893Ser
XM_011540044.1:c.8542A>T XP_011538346.1:p.Thr2848Ser
XM_011540045.1:c.8677A>T XP_011538347.1:p.Thr2893Ser
XM_011540046.1:c.8137A>T XP_011538348.1:p.Thr2713Ser
XM_011540047.1:c.7495A>T XP_011538349.1:p.Thr2499Ser
XM_011540052.1:c.5005A>T XP_011538354.1:p.Thr1669Ser
NM_022124.6:c.8482A>T MANE Select NP_071407.4:p.Thr2828Ser