Canonical Allele Identifier: CA2840853431

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800577G>T , CM000672.2:g.71800577G>T	GRCh38
NC_000010.10:g.73560334G>T , CM000672.1:g.73560334G>T	GRCh37
NC_000010.9:g.73230340G>T	NCBI36
NG_008835.1:g.408631G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7363-59G>T MANE Select	ENSP00000224721.9:n.7363-59G>T
ENST00000642965.1:c.1296-59G>T	ENSP00000495222.1:n.1296-59G>T
ENST00000647092.1:c.960-59G>T	ENSP00000495176.1:n.960-59G>T
ENST00000224721.10:c.7378-59G>T	ENSP00000224721.8:n.7378-59G>T
ENST00000398788.4:c.643-59G>T	ENSP00000381768.3:n.643-59G>T
ENST00000475158.1:n.899-59G>T
ENST00000619887.4:c.643-59G>T	ENSP00000478374.1:n.643-59G>T
ENST00000622827.4:c.7363-59G>T	ENSP00000483211.1:n.7363-59G>T
NM_001171933.1:c.643-59G>T	NP_001165404.1:n.643-59G>T
NM_001171934.1:c.643-59G>T	NP_001165405.1:n.643-59G>T
NM_022124.5:c.7363-59G>T	NP_071407.4:n.7363-59G>T
XM_006717940.2:c.7558-59G>T	XP_006718003.1:n.7558-59G>T
XM_006717942.2:c.7492-59G>T	XP_006718005.1:n.7492-59G>T
XM_011540039.1:c.7555-59G>T	XP_011538341.1:n.7555-59G>T
XM_011540040.1:c.7552-59G>T	XP_011538342.1:n.7552-59G>T
XM_011540041.1:c.7498-59G>T	XP_011538343.1:n.7498-59G>T
XM_011540042.1:c.7468-59G>T	XP_011538344.1:n.7468-59G>T
XM_011540043.1:c.7558-59G>T	XP_011538345.1:n.7558-59G>T
XM_011540044.1:c.7423-59G>T	XP_011538346.1:n.7423-59G>T
XM_011540045.1:c.7558-59G>T	XP_011538347.1:n.7558-59G>T
XM_011540046.1:c.7018-59G>T	XP_011538348.1:n.7018-59G>T
XM_011540047.1:c.6376-59G>T	XP_011538349.1:n.6376-59G>T
XM_011540052.1:c.3886-59G>T	XP_011538354.1:n.3886-59G>T
NM_022124.6:c.7363-59G>T MANE Select	NP_071407.4:n.7363-59G>T