Canonical Allele Identifier: CA377160668

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73562745G>T (hg19) ; chr10:g.71802988G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71802988G>T , CM000672.2:g.71802988G>T	GRCh38
NC_000010.10:g.73562745G>T , CM000672.1:g.73562745G>T	GRCh37
NC_000010.9:g.73232751G>T	NCBI36
NG_008835.1:g.411042G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7573G>T MANE Select	ENSP00000224721.9:p.Gly2525Cys
ENST00000642965.1:c.1506G>T	ENSP00000495222.1:n.1506G>T
ENST00000647092.1:c.1170G>T	ENSP00000495176.1:n.1170G>T
ENST00000224721.10:c.7588G>T	ENSP00000224721.8:p.Gly2530Cys
ENST00000398788.4:c.853G>T	ENSP00000381768.3:p.Gly285Cys
ENST00000475158.1:n.1109G>T
ENST00000619887.4:c.853G>T	ENSP00000478374.1:p.Gly285Cys
ENST00000622827.4:c.7573G>T	ENSP00000483211.1:p.Gly2525Cys
NM_001171933.1:c.853G>T	NP_001165404.1:p.Gly285Cys
NM_001171934.1:c.853G>T	NP_001165405.1:p.Gly285Cys
NM_022124.5:c.7573G>T	NP_071407.4:p.Gly2525Cys
XM_006717940.2:c.7768G>T	XP_006718003.1:p.Gly2590Cys
XM_006717942.2:c.7702G>T	XP_006718005.1:p.Gly2568Cys
XM_011540039.1:c.7765G>T	XP_011538341.1:p.Gly2589Cys
XM_011540040.1:c.7762G>T	XP_011538342.1:p.Gly2588Cys
XM_011540041.1:c.7708G>T	XP_011538343.1:p.Gly2570Cys
XM_011540042.1:c.7678G>T	XP_011538344.1:p.Gly2560Cys
XM_011540043.1:c.7768G>T	XP_011538345.1:p.Gly2590Cys
XM_011540044.1:c.7633G>T	XP_011538346.1:p.Gly2545Cys
XM_011540045.1:c.7768G>T	XP_011538347.1:p.Gly2590Cys
XM_011540046.1:c.7228G>T	XP_011538348.1:p.Gly2410Cys
XM_011540047.1:c.6586G>T	XP_011538349.1:p.Gly2196Cys
XM_011540052.1:c.4096G>T	XP_011538354.1:p.Gly1366Cys
NM_022124.6:c.7573G>T MANE Select	NP_071407.4:p.Gly2525Cys