Canonical Allele Identifier: CA470062257

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73560425G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800668G>T , CM000672.2:g.71800668G>T	GRCh38
NC_000010.10:g.73560425G>T , CM000672.1:g.73560425G>T	GRCh37
NC_000010.9:g.73230431G>T	NCBI36
NG_008835.1:g.408722G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7395G>T MANE Select	ENSP00000224721.9:p.Arg2465=
ENST00000642965.1:c.1328G>T	ENSP00000495222.1:n.1328G>T
ENST00000647092.1:c.992G>T	ENSP00000495176.1:n.992G>T
ENST00000224721.10:c.7410G>T	ENSP00000224721.8:p.Arg2470=
ENST00000398788.4:c.675G>T	ENSP00000381768.3:p.Arg225=
ENST00000475158.1:n.931G>T
ENST00000619887.4:c.675G>T	ENSP00000478374.1:p.Arg225=
ENST00000622827.4:c.7395G>T	ENSP00000483211.1:p.Arg2465=
NM_001171933.1:c.675G>T	NP_001165404.1:p.Arg225=
NM_001171934.1:c.675G>T	NP_001165405.1:p.Arg225=
NM_022124.5:c.7395G>T	NP_071407.4:p.Arg2465=
XM_006717940.2:c.7590G>T	XP_006718003.1:p.Arg2530=
XM_006717942.2:c.7524G>T	XP_006718005.1:p.Arg2508=
XM_011540039.1:c.7587G>T	XP_011538341.1:p.Arg2529=
XM_011540040.1:c.7584G>T	XP_011538342.1:p.Arg2528=
XM_011540041.1:c.7530G>T	XP_011538343.1:p.Arg2510=
XM_011540042.1:c.7500G>T	XP_011538344.1:p.Arg2500=
XM_011540043.1:c.7590G>T	XP_011538345.1:p.Arg2530=
XM_011540044.1:c.7455G>T	XP_011538346.1:p.Arg2485=
XM_011540045.1:c.7590G>T	XP_011538347.1:p.Arg2530=
XM_011540046.1:c.7050G>T	XP_011538348.1:p.Arg2350=
XM_011540047.1:c.6408G>T	XP_011538349.1:p.Arg2136=
XM_011540052.1:c.3918G>T	XP_011538354.1:p.Arg1306=
NM_022124.6:c.7395G>T MANE Select	NP_071407.4:p.Arg2465=