Canonical Allele Identifier: CA1918879380

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800632C= , CM000672.2:g.71800632C=	GRCh38
NC_000010.10:g.73560389C= , CM000672.1:g.73560389C=	GRCh37
NC_000010.9:g.73230395C=	NCBI36
NG_008835.1:g.408686C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7363-4C= MANE Select	ENSP00000224721.9:n.7363-4C=
ENST00000642965.1:c.1296-4C=	ENSP00000495222.1:n.1296-4C=
ENST00000647092.1:c.960-4C=	ENSP00000495176.1:n.960-4C=
ENST00000224721.10:c.7378-4C=	ENSP00000224721.8:n.7378-4C=
ENST00000398788.4:c.643-4C=	ENSP00000381768.3:n.643-4C=
ENST00000475158.1:n.899-4C=
ENST00000619887.4:c.643-4C=	ENSP00000478374.1:n.643-4C=
ENST00000622827.4:c.7363-4C=	ENSP00000483211.1:n.7363-4C=
NM_001171933.1:c.643-4C=	NP_001165404.1:n.643-4C=
NM_001171934.1:c.643-4C=	NP_001165405.1:n.643-4C=
NM_022124.5:c.7363-4C=	NP_071407.4:n.7363-4C=
XM_006717940.2:c.7558-4C=	XP_006718003.1:n.7558-4C=
XM_006717942.2:c.7492-4C=	XP_006718005.1:n.7492-4C=
XM_011540039.1:c.7555-4C=	XP_011538341.1:n.7555-4C=
XM_011540040.1:c.7552-4C=	XP_011538342.1:n.7552-4C=
XM_011540041.1:c.7498-4C=	XP_011538343.1:n.7498-4C=
XM_011540042.1:c.7468-4C=	XP_011538344.1:n.7468-4C=
XM_011540043.1:c.7558-4C=	XP_011538345.1:n.7558-4C=
XM_011540044.1:c.7423-4C=	XP_011538346.1:n.7423-4C=
XM_011540045.1:c.7558-4C=	XP_011538347.1:n.7558-4C=
XM_011540046.1:c.7018-4C=	XP_011538348.1:n.7018-4C=
XM_011540047.1:c.6376-4C=	XP_011538349.1:n.6376-4C=
XM_011540052.1:c.3886-4C=	XP_011538354.1:n.3886-4C=
NM_022124.6:c.7363-4C= MANE Select	NP_071407.4:n.7363-4C=