Canonical Allele Identifier: CA1918878489

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798530C= , CM000672.2:g.71798530C=	GRCh38
NC_000010.10:g.73558287C= , CM000672.1:g.73558287C=	GRCh37
NC_000010.9:g.73228293C=	NCBI36
NG_008835.1:g.406584C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7006C= MANE Select	ENSP00000224721.9:p.Leu2336=
ENST00000642965.1:c.939C=	ENSP00000495222.1:n.939C=
ENST00000647092.1:c.603C=	ENSP00000495176.1:n.603C=
ENST00000224721.10:c.7021C=	ENSP00000224721.8:p.Leu2341=
ENST00000398788.4:c.286C=	ENSP00000381768.3:p.Leu96=
ENST00000475158.1:n.542C=
ENST00000619887.4:c.286C=	ENSP00000478374.1:p.Leu96=
ENST00000622827.4:c.7006C=	ENSP00000483211.1:p.Leu2336=
NM_001171933.1:c.286C=	NP_001165404.1:p.Leu96=
NM_001171934.1:c.286C=	NP_001165405.1:p.Leu96=
NM_022124.5:c.7006C=	NP_071407.4:p.Leu2336=
XM_006717940.2:c.7201C=	XP_006718003.1:p.Leu2401=
XM_006717942.2:c.7135C=	XP_006718005.1:p.Leu2379=
XM_011540039.1:c.7198C=	XP_011538341.1:p.Leu2400=
XM_011540040.1:c.7195C=	XP_011538342.1:p.Leu2399=
XM_011540041.1:c.7141C=	XP_011538343.1:p.Leu2381=
XM_011540042.1:c.7111C=	XP_011538344.1:p.Leu2371=
XM_011540043.1:c.7201C=	XP_011538345.1:p.Leu2401=
XM_011540044.1:c.7066C=	XP_011538346.1:p.Leu2356=
XM_011540045.1:c.7201C=	XP_011538347.1:p.Leu2401=
XM_011540046.1:c.6661C=	XP_011538348.1:p.Leu2221=
XM_011540047.1:c.6019C=	XP_011538349.1:p.Leu2007=
XM_011540052.1:c.3529C=	XP_011538354.1:p.Leu1177=
NM_022124.6:c.7006C= MANE Select	NP_071407.4:p.Leu2336=