Canonical Allele Identifier: CA1918878927
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71799560A= , CM000672.2:g.71799560A= GRCh38
NC_000010.10:g.73559317A= , CM000672.1:g.73559317A= GRCh37
NC_000010.9:g.73229323A= NCBI36
NG_008835.1:g.407614A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.7293A= MANE Select ENSP00000224721.9:p.Ser2431=
ENST00000642965.1:c.1226A= ENSP00000495222.1:n.1226A=
ENST00000647092.1:c.890A= ENSP00000495176.1:n.890A=
ENST00000224721.10:c.7308A= ENSP00000224721.8:p.Ser2436=
ENST00000398788.4:c.573A= ENSP00000381768.3:p.Ser191=
ENST00000475158.1:n.829A=
ENST00000619887.4:c.573A= ENSP00000478374.1:p.Ser191=
ENST00000622827.4:c.7293A= ENSP00000483211.1:p.Ser2431=
NM_001171933.1:c.573A= NP_001165404.1:p.Ser191=
NM_001171934.1:c.573A= NP_001165405.1:p.Ser191=
NM_022124.5:c.7293A= NP_071407.4:p.Ser2431=
XM_006717940.2:c.7488A= XP_006718003.1:p.Ser2496=
XM_006717942.2:c.7422A= XP_006718005.1:p.Ser2474=
XM_011540039.1:c.7485A= XP_011538341.1:p.Ser2495=
XM_011540040.1:c.7482A= XP_011538342.1:p.Ser2494=
XM_011540041.1:c.7428A= XP_011538343.1:p.Ser2476=
XM_011540042.1:c.7398A= XP_011538344.1:p.Ser2466=
XM_011540043.1:c.7488A= XP_011538345.1:p.Ser2496=
XM_011540044.1:c.7353A= XP_011538346.1:p.Ser2451=
XM_011540045.1:c.7488A= XP_011538347.1:p.Ser2496=
XM_011540046.1:c.6948A= XP_011538348.1:p.Ser2316=
XM_011540047.1:c.6306A= XP_011538349.1:p.Ser2102=
XM_011540052.1:c.3816A= XP_011538354.1:p.Ser1272=
NM_022124.6:c.7293A= MANE Select NP_071407.4:p.Ser2431=