Canonical Allele Identifier: CA209442263

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71811352C>T , CM000672.2:g.71811352C>T	GRCh38
NC_000010.10:g.73571109C>T , CM000672.1:g.73571109C>T	GRCh37
NC_000010.9:g.73241115C>T	NCBI36
NG_008835.1:g.419406C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.9115C>T MANE Select	ENSP00000224721.9:p.Arg3039Trp
ENST00000642965.1:c.3048C>T	ENSP00000495222.1:n.3048C>T
ENST00000647092.1:c.2712C>T	ENSP00000495176.1:n.2712C>T
ENST00000224721.10:c.9130C>T	ENSP00000224721.8:p.Arg3044Trp
ENST00000398788.4:c.2395C>T	ENSP00000381768.3:p.Arg799Trp
ENST00000475158.1:n.2651C>T
ENST00000619887.4:c.2395C>T	ENSP00000478374.1:p.Arg799Trp
ENST00000622827.4:c.9115C>T	ENSP00000483211.1:p.Arg3039Trp
NM_001171933.1:c.2395C>T	NP_001165404.1:p.Arg799Trp
NM_001171934.1:c.2395C>T	NP_001165405.1:p.Arg799Trp
NM_022124.5:c.9115C>T	NP_071407.4:p.Arg3039Trp
XM_006717940.2:c.9310C>T	XP_006718003.1:p.Arg3104Trp
XM_006717942.2:c.9244C>T	XP_006718005.1:p.Arg3082Trp
XM_011540039.1:c.9307C>T	XP_011538341.1:p.Arg3103Trp
XM_011540040.1:c.9304C>T	XP_011538342.1:p.Arg3102Trp
XM_011540041.1:c.9250C>T	XP_011538343.1:p.Arg3084Trp
XM_011540042.1:c.9220C>T	XP_011538344.1:p.Arg3074Trp
XM_011540043.1:c.9310C>T	XP_011538345.1:p.Arg3104Trp
XM_011540044.1:c.9175C>T	XP_011538346.1:p.Arg3059Trp
XM_011540045.1:c.9310C>T	XP_011538347.1:p.Arg3104Trp
XM_011540046.1:c.8770C>T	XP_011538348.1:p.Arg2924Trp
XM_011540047.1:c.8128C>T	XP_011538349.1:p.Arg2710Trp
XM_011540052.1:c.5638C>T	XP_011538354.1:p.Arg1880Trp
NM_022124.6:c.9115C>T MANE Select	NP_071407.4:p.Arg3039Trp