Canonical Allele Identifier: CA377159301
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71799540A>C , CM000672.2:g.71799540A>C GRCh38
NC_000010.10:g.73559297A>C , CM000672.1:g.73559297A>C GRCh37
NC_000010.9:g.73229303A>C NCBI36
NG_008835.1:g.407594A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.7273A>C MANE Select ENSP00000224721.9:p.Thr2425Pro
ENST00000642965.1:c.1206A>C ENSP00000495222.1:n.1206A>C
ENST00000647092.1:c.870A>C ENSP00000495176.1:n.870A>C
ENST00000224721.10:c.7288A>C ENSP00000224721.8:p.Thr2430Pro
ENST00000398788.4:c.553A>C ENSP00000381768.3:p.Thr185Pro
ENST00000475158.1:n.809A>C
ENST00000619887.4:c.553A>C ENSP00000478374.1:p.Thr185Pro
ENST00000622827.4:c.7273A>C ENSP00000483211.1:p.Thr2425Pro
NM_001171933.1:c.553A>C NP_001165404.1:p.Thr185Pro
NM_001171934.1:c.553A>C NP_001165405.1:p.Thr185Pro
NM_022124.5:c.7273A>C NP_071407.4:p.Thr2425Pro
XM_006717940.2:c.7468A>C XP_006718003.1:p.Thr2490Pro
XM_006717942.2:c.7402A>C XP_006718005.1:p.Thr2468Pro
XM_011540039.1:c.7465A>C XP_011538341.1:p.Thr2489Pro
XM_011540040.1:c.7462A>C XP_011538342.1:p.Thr2488Pro
XM_011540041.1:c.7408A>C XP_011538343.1:p.Thr2470Pro
XM_011540042.1:c.7378A>C XP_011538344.1:p.Thr2460Pro
XM_011540043.1:c.7468A>C XP_011538345.1:p.Thr2490Pro
XM_011540044.1:c.7333A>C XP_011538346.1:p.Thr2445Pro
XM_011540045.1:c.7468A>C XP_011538347.1:p.Thr2490Pro
XM_011540046.1:c.6928A>C XP_011538348.1:p.Thr2310Pro
XM_011540047.1:c.6286A>C XP_011538349.1:p.Thr2096Pro
XM_011540052.1:c.3796A>C XP_011538354.1:p.Thr1266Pro
NM_022124.6:c.7273A>C MANE Select NP_071407.4:p.Thr2425Pro