Canonical Allele Identifier: CA1918878920
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71799540_71799542delinsACT , CM000672.2:g.71799540_71799542delinsACT GRCh38
NC_000010.10:g.73559297_73559299delinsACT , CM000672.1:g.73559297_73559299delinsACT GRCh37
NC_000010.9:g.73229303_73229305delinsACT NCBI36
NG_008835.1:g.407594_407596delinsACT

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.7273_7275delinsACT MANE Select ENSP00000224721.9:p.Thr2425=
ENST00000642965.1:c.1206_1208delinsACT ENSP00000495222.1:n.1206_1208delinsACT
ENST00000647092.1:c.870_872delinsACT ENSP00000495176.1:n.870_872delinsACT
ENST00000224721.10:c.7288_7290delinsACT ENSP00000224721.8:p.Thr2430=
ENST00000398788.4:c.553_555delinsACT ENSP00000381768.3:p.Thr185=
ENST00000475158.1:n.809_811delinsACT
ENST00000619887.4:c.553_555delinsACT ENSP00000478374.1:p.Thr185=
ENST00000622827.4:c.7273_7275delinsACT ENSP00000483211.1:p.Thr2425=
NM_001171933.1:c.553_555delinsACT NP_001165404.1:p.Thr185=
NM_001171934.1:c.553_555delinsACT NP_001165405.1:p.Thr185=
NM_022124.5:c.7273_7275delinsACT NP_071407.4:p.Thr2425=
XM_006717940.2:c.7468_7470delinsACT XP_006718003.1:p.Thr2490=
XM_006717942.2:c.7402_7404delinsACT XP_006718005.1:p.Thr2468=
XM_011540039.1:c.7465_7467delinsACT XP_011538341.1:p.Thr2489=
XM_011540040.1:c.7462_7464delinsACT XP_011538342.1:p.Thr2488=
XM_011540041.1:c.7408_7410delinsACT XP_011538343.1:p.Thr2470=
XM_011540042.1:c.7378_7380delinsACT XP_011538344.1:p.Thr2460=
XM_011540043.1:c.7468_7470delinsACT XP_011538345.1:p.Thr2490=
XM_011540044.1:c.7333_7335delinsACT XP_011538346.1:p.Thr2445=
XM_011540045.1:c.7468_7470delinsACT XP_011538347.1:p.Thr2490=
XM_011540046.1:c.6928_6930delinsACT XP_011538348.1:p.Thr2310=
XM_011540047.1:c.6286_6288delinsACT XP_011538349.1:p.Thr2096=
XM_011540052.1:c.3796_3798delinsACT XP_011538354.1:p.Thr1266=
NM_022124.6:c.7273_7275delinsACT MANE Select NP_071407.4:p.Thr2425=