Canonical Allele Identifier: CA1918886553

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807614G= , CM000672.2:g.71807614G=	GRCh38
NC_000010.10:g.73567371G= , CM000672.1:g.73567371G=	GRCh37
NC_000010.9:g.73237377G=	NCBI36
NG_008835.1:g.415668G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8407G= MANE Select	ENSP00000224721.9:p.Val2803=
ENST00000642965.1:c.2340G=	ENSP00000495222.1:n.2340G=
ENST00000647092.1:c.2004G=	ENSP00000495176.1:n.2004G=
ENST00000224721.10:c.8422G=	ENSP00000224721.8:p.Val2808=
ENST00000398788.4:c.1687G=	ENSP00000381768.3:p.Val563=
ENST00000475158.1:n.1943G=
ENST00000619887.4:c.1687G=	ENSP00000478374.1:p.Val563=
ENST00000622827.4:c.8407G=	ENSP00000483211.1:p.Val2803=
NM_001171933.1:c.1687G=	NP_001165404.1:p.Val563=
NM_001171934.1:c.1687G=	NP_001165405.1:p.Val563=
NM_022124.5:c.8407G=	NP_071407.4:p.Val2803=
XM_006717940.2:c.8602G=	XP_006718003.1:p.Val2868=
XM_006717942.2:c.8536G=	XP_006718005.1:p.Val2846=
XM_011540039.1:c.8599G=	XP_011538341.1:p.Val2867=
XM_011540040.1:c.8596G=	XP_011538342.1:p.Val2866=
XM_011540041.1:c.8542G=	XP_011538343.1:p.Val2848=
XM_011540042.1:c.8512G=	XP_011538344.1:p.Val2838=
XM_011540043.1:c.8602G=	XP_011538345.1:p.Val2868=
XM_011540044.1:c.8467G=	XP_011538346.1:p.Val2823=
XM_011540045.1:c.8602G=	XP_011538347.1:p.Val2868=
XM_011540046.1:c.8062G=	XP_011538348.1:p.Val2688=
XM_011540047.1:c.7420G=	XP_011538349.1:p.Val2474=
XM_011540052.1:c.4930G=	XP_011538354.1:p.Val1644=
NM_022124.6:c.8407G= MANE Select	NP_071407.4:p.Val2803=