Canonical Allele Identifier: CA3174440491

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71809867A= , CM000672.2:g.71809867A=	GRCh38
NC_000010.10:g.73569624A= , CM000672.1:g.73569624A=	GRCh37
NC_000010.9:g.73239630A=	NCBI36
NG_008835.1:g.417921A=

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.8770A= MANE Select	NP_071407.4:p.Ser2924=
ENST00000224721.12:c.8770A= MANE Select	ENSP00000224721.9:p.Ser2924=
NM_001171933.1:c.2050A=	NP_001165404.1:p.Ser684=
NM_001171934.1:c.2050A=	NP_001165405.1:p.Ser684=
NM_022124.5:c.8770A=	NP_071407.4:p.Ser2924=
ENST00000224721.10:c.8785A=	ENSP00000224721.8:p.Ser2929=
ENST00000398788.4:c.2050A=	ENSP00000381768.3:p.Ser684=
ENST00000475158.1:n.2306A=
ENST00000619887.4:c.2050A=	ENSP00000478374.1:p.Ser684=
ENST00000622827.4:c.8770A=	ENSP00000483211.1:p.Ser2924=
ENST00000642965.1:c.2703A=	ENSP00000495222.1:n.2703A=
ENST00000647092.1:c.2367A=	ENSP00000495176.1:n.2367A=
XM_006717940.2:c.8965A=	XP_006718003.1:p.Ser2989=
XM_006717942.2:c.8899A=	XP_006718005.1:p.Ser2967=
XM_011540039.1:c.8962A=	XP_011538341.1:p.Ser2988=
XM_011540040.1:c.8959A=	XP_011538342.1:p.Ser2987=
XM_011540041.1:c.8905A=	XP_011538343.1:p.Ser2969=
XM_011540042.1:c.8875A=	XP_011538344.1:p.Ser2959=
XM_011540043.1:c.8965A=	XP_011538345.1:p.Ser2989=
XM_011540044.1:c.8830A=	XP_011538346.1:p.Ser2944=
XM_011540045.1:c.8965A=	XP_011538347.1:p.Ser2989=
XM_011540046.1:c.8425A=	XP_011538348.1:p.Ser2809=
XM_011540047.1:c.7783A=	XP_011538349.1:p.Ser2595=
XM_011540052.1:c.5293A=	XP_011538354.1:p.Ser1765=