Canonical Allele Identifier: CA2515864352

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71803205C>T , CM000672.2:g.71803205C>T	GRCh38
NC_000010.10:g.73562962C>T , CM000672.1:g.73562962C>T	GRCh37
NC_000010.9:g.73232968C>T	NCBI36
NG_008835.1:g.411259C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7661-4C>T MANE Select	ENSP00000224721.9:n.7661-4C>T
ENST00000642965.1:c.1594-4C>T	ENSP00000495222.1:n.1594-4C>T
ENST00000647092.1:c.1258-4C>T	ENSP00000495176.1:n.1258-4C>T
ENST00000224721.10:c.7676-4C>T	ENSP00000224721.8:n.7676-4C>T
ENST00000398788.4:c.941-4C>T	ENSP00000381768.3:n.941-4C>T
ENST00000475158.1:n.1197-4C>T
ENST00000619887.4:c.941-4C>T	ENSP00000478374.1:n.941-4C>T
ENST00000622827.4:c.7661-4C>T	ENSP00000483211.1:n.7661-4C>T
NM_001171933.1:c.941-4C>T	NP_001165404.1:n.941-4C>T
NM_001171934.1:c.941-4C>T	NP_001165405.1:n.941-4C>T
NM_022124.5:c.7661-4C>T	NP_071407.4:n.7661-4C>T
XM_006717940.2:c.7856-4C>T	XP_006718003.1:n.7856-4C>T
XM_006717942.2:c.7790-4C>T	XP_006718005.1:n.7790-4C>T
XM_011540039.1:c.7853-4C>T	XP_011538341.1:n.7853-4C>T
XM_011540040.1:c.7850-4C>T	XP_011538342.1:n.7850-4C>T
XM_011540041.1:c.7796-4C>T	XP_011538343.1:n.7796-4C>T
XM_011540042.1:c.7766-4C>T	XP_011538344.1:n.7766-4C>T
XM_011540043.1:c.7856-4C>T	XP_011538345.1:n.7856-4C>T
XM_011540044.1:c.7721-4C>T	XP_011538346.1:n.7721-4C>T
XM_011540045.1:c.7856-4C>T	XP_011538347.1:n.7856-4C>T
XM_011540046.1:c.7316-4C>T	XP_011538348.1:n.7316-4C>T
XM_011540047.1:c.6674-4C>T	XP_011538349.1:n.6674-4C>T
XM_011540052.1:c.4184-4C>T	XP_011538354.1:n.4184-4C>T
NM_022124.6:c.7661-4C>T MANE Select	NP_071407.4:n.7661-4C>T