Canonical Allele Identifier: CA470062200

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558334A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798577A>T , CM000672.2:g.71798577A>T	GRCh38
NC_000010.10:g.73558334A>T , CM000672.1:g.73558334A>T	GRCh37
NC_000010.9:g.73228340A>T	NCBI36
NG_008835.1:g.406631A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7053A>T MANE Select	ENSP00000224721.9:p.Ala2351=
ENST00000642965.1:c.986A>T	ENSP00000495222.1:n.986A>T
ENST00000647092.1:c.650A>T	ENSP00000495176.1:n.650A>T
ENST00000224721.10:c.7068A>T	ENSP00000224721.8:p.Ala2356=
ENST00000398788.4:c.333A>T	ENSP00000381768.3:p.Ala111=
ENST00000475158.1:n.589A>T
ENST00000619887.4:c.333A>T	ENSP00000478374.1:p.Ala111=
ENST00000622827.4:c.7053A>T	ENSP00000483211.1:p.Ala2351=
NM_001171933.1:c.333A>T	NP_001165404.1:p.Ala111=
NM_001171934.1:c.333A>T	NP_001165405.1:p.Ala111=
NM_022124.5:c.7053A>T	NP_071407.4:p.Ala2351=
XM_006717940.2:c.7248A>T	XP_006718003.1:p.Ala2416=
XM_006717942.2:c.7182A>T	XP_006718005.1:p.Ala2394=
XM_011540039.1:c.7245A>T	XP_011538341.1:p.Ala2415=
XM_011540040.1:c.7242A>T	XP_011538342.1:p.Ala2414=
XM_011540041.1:c.7188A>T	XP_011538343.1:p.Ala2396=
XM_011540042.1:c.7158A>T	XP_011538344.1:p.Ala2386=
XM_011540043.1:c.7248A>T	XP_011538345.1:p.Ala2416=
XM_011540044.1:c.7113A>T	XP_011538346.1:p.Ala2371=
XM_011540045.1:c.7248A>T	XP_011538347.1:p.Ala2416=
XM_011540046.1:c.6708A>T	XP_011538348.1:p.Ala2236=
XM_011540047.1:c.6066A>T	XP_011538349.1:p.Ala2022=
XM_011540052.1:c.3576A>T	XP_011538354.1:p.Ala1192=
NM_022124.6:c.7053A>T MANE Select	NP_071407.4:p.Ala2351=