Canonical Allele Identifier: CA2840293842
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71798492dup , CM000672.2:g.71798492dup GRCh38
NC_000010.10:g.73558249dup , CM000672.1:g.73558249dup GRCh37
NC_000010.9:g.73228255dup NCBI36
NG_008835.1:g.406546dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.6968dup MANE Select ENSP00000224721.9:p.Asp2324Ter
ENST00000642965.1:c.901dup ENSP00000495222.1:n.901dup
ENST00000647092.1:c.565dup ENSP00000495176.1:n.565dup
ENST00000224721.10:c.6983dup ENSP00000224721.8:p.Asp2329Ter
ENST00000398788.4:c.248dup ENSP00000381768.3:p.Asp84Ter
ENST00000475158.1:n.504dup
ENST00000619887.4:c.248dup ENSP00000478374.1:p.Asp84Ter
ENST00000622827.4:c.6968dup ENSP00000483211.1:p.Asp2324Ter
NM_001171933.1:c.248dup NP_001165404.1:p.Asp84Ter
NM_001171934.1:c.248dup NP_001165405.1:p.Asp84Ter
NM_022124.5:c.6968dup NP_071407.4:p.Asp2324Ter
XM_006717940.2:c.7163dup XP_006718003.1:p.Asp2389Ter
XM_006717942.2:c.7097dup XP_006718005.1:p.Asp2367Ter
XM_011540039.1:c.7160dup XP_011538341.1:p.Asp2388Ter
XM_011540040.1:c.7157dup XP_011538342.1:p.Asp2387Ter
XM_011540041.1:c.7103dup XP_011538343.1:p.Asp2369Ter
XM_011540042.1:c.7073dup XP_011538344.1:p.Asp2359Ter
XM_011540043.1:c.7163dup XP_011538345.1:p.Asp2389Ter
XM_011540044.1:c.7028dup XP_011538346.1:p.Asp2344Ter
XM_011540045.1:c.7163dup XP_011538347.1:p.Asp2389Ter
XM_011540046.1:c.6623dup XP_011538348.1:p.Asp2209Ter
XM_011540047.1:c.5981dup XP_011538349.1:p.Asp1995Ter
XM_011540052.1:c.3491dup XP_011538354.1:p.Asp1165Ter
NM_022124.6:c.6968dup MANE Select NP_071407.4:p.Asp2324Ter