Canonical Allele Identifier: CA470282098

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73559305T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799548T>C , CM000672.2:g.71799548T>C	GRCh38
NC_000010.10:g.73559305T>C , CM000672.1:g.73559305T>C	GRCh37
NC_000010.9:g.73229311T>C	NCBI36
NG_008835.1:g.407602T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7281T>C MANE Select	ENSP00000224721.9:p.Thr2427=
ENST00000642965.1:c.1214T>C	ENSP00000495222.1:n.1214T>C
ENST00000647092.1:c.878T>C	ENSP00000495176.1:n.878T>C
ENST00000224721.10:c.7296T>C	ENSP00000224721.8:p.Thr2432=
ENST00000398788.4:c.561T>C	ENSP00000381768.3:p.Thr187=
ENST00000475158.1:n.817T>C
ENST00000619887.4:c.561T>C	ENSP00000478374.1:p.Thr187=
ENST00000622827.4:c.7281T>C	ENSP00000483211.1:p.Thr2427=
NM_001171933.1:c.561T>C	NP_001165404.1:p.Thr187=
NM_001171934.1:c.561T>C	NP_001165405.1:p.Thr187=
NM_022124.5:c.7281T>C	NP_071407.4:p.Thr2427=
XM_006717940.2:c.7476T>C	XP_006718003.1:p.Thr2492=
XM_006717942.2:c.7410T>C	XP_006718005.1:p.Thr2470=
XM_011540039.1:c.7473T>C	XP_011538341.1:p.Thr2491=
XM_011540040.1:c.7470T>C	XP_011538342.1:p.Thr2490=
XM_011540041.1:c.7416T>C	XP_011538343.1:p.Thr2472=
XM_011540042.1:c.7386T>C	XP_011538344.1:p.Thr2462=
XM_011540043.1:c.7476T>C	XP_011538345.1:p.Thr2492=
XM_011540044.1:c.7341T>C	XP_011538346.1:p.Thr2447=
XM_011540045.1:c.7476T>C	XP_011538347.1:p.Thr2492=
XM_011540046.1:c.6936T>C	XP_011538348.1:p.Thr2312=
XM_011540047.1:c.6294T>C	XP_011538349.1:p.Thr2098=
XM_011540052.1:c.3804T>C	XP_011538354.1:p.Thr1268=
NM_022124.6:c.7281T>C MANE Select	NP_071407.4:p.Thr2427=