Canonical Allele Identifier: CA377159339
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71799550A>T , CM000672.2:g.71799550A>T GRCh38
NC_000010.10:g.73559307A>T , CM000672.1:g.73559307A>T GRCh37
NC_000010.9:g.73229313A>T NCBI36
NG_008835.1:g.407604A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.7283A>T MANE Select ENSP00000224721.9:p.Asp2428Val
ENST00000642965.1:c.1216A>T ENSP00000495222.1:n.1216A>T
ENST00000647092.1:c.880A>T ENSP00000495176.1:n.880A>T
ENST00000224721.10:c.7298A>T ENSP00000224721.8:p.Asp2433Val
ENST00000398788.4:c.563A>T ENSP00000381768.3:p.Asp188Val
ENST00000475158.1:n.819A>T
ENST00000619887.4:c.563A>T ENSP00000478374.1:p.Asp188Val
ENST00000622827.4:c.7283A>T ENSP00000483211.1:p.Asp2428Val
NM_001171933.1:c.563A>T NP_001165404.1:p.Asp188Val
NM_001171934.1:c.563A>T NP_001165405.1:p.Asp188Val
NM_022124.5:c.7283A>T NP_071407.4:p.Asp2428Val
XM_006717940.2:c.7478A>T XP_006718003.1:p.Asp2493Val
XM_006717942.2:c.7412A>T XP_006718005.1:p.Asp2471Val
XM_011540039.1:c.7475A>T XP_011538341.1:p.Asp2492Val
XM_011540040.1:c.7472A>T XP_011538342.1:p.Asp2491Val
XM_011540041.1:c.7418A>T XP_011538343.1:p.Asp2473Val
XM_011540042.1:c.7388A>T XP_011538344.1:p.Asp2463Val
XM_011540043.1:c.7478A>T XP_011538345.1:p.Asp2493Val
XM_011540044.1:c.7343A>T XP_011538346.1:p.Asp2448Val
XM_011540045.1:c.7478A>T XP_011538347.1:p.Asp2493Val
XM_011540046.1:c.6938A>T XP_011538348.1:p.Asp2313Val
XM_011540047.1:c.6296A>T XP_011538349.1:p.Asp2099Val
XM_011540052.1:c.3806A>T XP_011538354.1:p.Asp1269Val
NM_022124.6:c.7283A>T MANE Select NP_071407.4:p.Asp2428Val