Canonical Allele Identifier: CA470062064

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558238A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798481A>T , CM000672.2:g.71798481A>T	GRCh38
NC_000010.10:g.73558238A>T , CM000672.1:g.73558238A>T	GRCh37
NC_000010.9:g.73228244A>T	NCBI36
NG_008835.1:g.406535A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6957A>T MANE Select	ENSP00000224721.9:p.Ala2319=
ENST00000642965.1:c.890A>T	ENSP00000495222.1:n.890A>T
ENST00000647092.1:c.554A>T	ENSP00000495176.1:n.554A>T
ENST00000224721.10:c.6972A>T	ENSP00000224721.8:p.Ala2324=
ENST00000398788.4:c.237A>T	ENSP00000381768.3:p.Ala79=
ENST00000475158.1:n.493A>T
ENST00000619887.4:c.237A>T	ENSP00000478374.1:p.Ala79=
ENST00000622827.4:c.6957A>T	ENSP00000483211.1:p.Ala2319=
NM_001171933.1:c.237A>T	NP_001165404.1:p.Ala79=
NM_001171934.1:c.237A>T	NP_001165405.1:p.Ala79=
NM_022124.5:c.6957A>T	NP_071407.4:p.Ala2319=
XM_006717940.2:c.7152A>T	XP_006718003.1:p.Ala2384=
XM_006717942.2:c.7086A>T	XP_006718005.1:p.Ala2362=
XM_011540039.1:c.7149A>T	XP_011538341.1:p.Ala2383=
XM_011540040.1:c.7146A>T	XP_011538342.1:p.Ala2382=
XM_011540041.1:c.7092A>T	XP_011538343.1:p.Ala2364=
XM_011540042.1:c.7062A>T	XP_011538344.1:p.Ala2354=
XM_011540043.1:c.7152A>T	XP_011538345.1:p.Ala2384=
XM_011540044.1:c.7017A>T	XP_011538346.1:p.Ala2339=
XM_011540045.1:c.7152A>T	XP_011538347.1:p.Ala2384=
XM_011540046.1:c.6612A>T	XP_011538348.1:p.Ala2204=
XM_011540047.1:c.5970A>T	XP_011538349.1:p.Ala1990=
XM_011540052.1:c.3480A>T	XP_011538354.1:p.Ala1160=
NM_022124.6:c.6957A>T MANE Select	NP_071407.4:p.Ala2319=