Canonical Allele Identifier: CA1918878401
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71798357A= , CM000672.2:g.71798357A= GRCh38
NC_000010.10:g.73558114A= , CM000672.1:g.73558114A= GRCh37
NC_000010.9:g.73228120A= NCBI36
NG_008835.1:g.406411A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.6833A= MANE Select ENSP00000224721.9:p.Lys2278=
ENST00000642965.1:c.766A= ENSP00000495222.1:n.766A=
ENST00000647092.1:c.430A= ENSP00000495176.1:n.430A=
ENST00000224721.10:c.6848A= ENSP00000224721.8:p.Lys2283=
ENST00000398788.4:c.113A= ENSP00000381768.3:p.Lys38=
ENST00000475158.1:n.369A=
ENST00000619887.4:c.113A= ENSP00000478374.1:p.Lys38=
ENST00000622827.4:c.6833A= ENSP00000483211.1:p.Lys2278=
NM_001171933.1:c.113A= NP_001165404.1:p.Lys38=
NM_001171934.1:c.113A= NP_001165405.1:p.Lys38=
NM_022124.5:c.6833A= NP_071407.4:p.Lys2278=
XM_006717940.2:c.7028A= XP_006718003.1:p.Lys2343=
XM_006717942.2:c.6962A= XP_006718005.1:p.Lys2321=
XM_011540039.1:c.7025A= XP_011538341.1:p.Lys2342=
XM_011540040.1:c.7022A= XP_011538342.1:p.Lys2341=
XM_011540041.1:c.6968A= XP_011538343.1:p.Lys2323=
XM_011540042.1:c.6938A= XP_011538344.1:p.Lys2313=
XM_011540043.1:c.7028A= XP_011538345.1:p.Lys2343=
XM_011540044.1:c.6893A= XP_011538346.1:p.Lys2298=
XM_011540045.1:c.7028A= XP_011538347.1:p.Lys2343=
XM_011540046.1:c.6488A= XP_011538348.1:p.Lys2163=
XM_011540047.1:c.5846A= XP_011538349.1:p.Lys1949=
XM_011540052.1:c.3356A= XP_011538354.1:p.Lys1119=
NM_022124.6:c.6833A= MANE Select NP_071407.4:p.Lys2278=