Canonical Allele Identifier: CA1918878483

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798521T= , CM000672.2:g.71798521T=	GRCh38
NC_000010.10:g.73558278T= , CM000672.1:g.73558278T=	GRCh37
NC_000010.9:g.73228284T=	NCBI36
NG_008835.1:g.406575T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6997T= MANE Select	ENSP00000224721.9:p.Tyr2333=
ENST00000642965.1:c.930T=	ENSP00000495222.1:n.930T=
ENST00000647092.1:c.594T=	ENSP00000495176.1:n.594T=
ENST00000224721.10:c.7012T=	ENSP00000224721.8:p.Tyr2338=
ENST00000398788.4:c.277T=	ENSP00000381768.3:p.Tyr93=
ENST00000475158.1:n.533T=
ENST00000619887.4:c.277T=	ENSP00000478374.1:p.Tyr93=
ENST00000622827.4:c.6997T=	ENSP00000483211.1:p.Tyr2333=
NM_001171933.1:c.277T=	NP_001165404.1:p.Tyr93=
NM_001171934.1:c.277T=	NP_001165405.1:p.Tyr93=
NM_022124.5:c.6997T=	NP_071407.4:p.Tyr2333=
XM_006717940.2:c.7192T=	XP_006718003.1:p.Tyr2398=
XM_006717942.2:c.7126T=	XP_006718005.1:p.Tyr2376=
XM_011540039.1:c.7189T=	XP_011538341.1:p.Tyr2397=
XM_011540040.1:c.7186T=	XP_011538342.1:p.Tyr2396=
XM_011540041.1:c.7132T=	XP_011538343.1:p.Tyr2378=
XM_011540042.1:c.7102T=	XP_011538344.1:p.Tyr2368=
XM_011540043.1:c.7192T=	XP_011538345.1:p.Tyr2398=
XM_011540044.1:c.7057T=	XP_011538346.1:p.Tyr2353=
XM_011540045.1:c.7192T=	XP_011538347.1:p.Tyr2398=
XM_011540046.1:c.6652T=	XP_011538348.1:p.Tyr2218=
XM_011540047.1:c.6010T=	XP_011538349.1:p.Tyr2004=
XM_011540052.1:c.3520T=	XP_011538354.1:p.Tyr1174=
NM_022124.6:c.6997T= MANE Select	NP_071407.4:p.Tyr2333=