Canonical Allele Identifier: CA470282489

Gene: CDH23

Linked Data

• dbSNP Id: rs1388089297
• MyVariant Identifiers: chr10:g.73567400A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807643A>T , CM000672.2:g.71807643A>T	GRCh38
NC_000010.10:g.73567400A>T , CM000672.1:g.73567400A>T	GRCh37
NC_000010.9:g.73237406A>T	NCBI36
NG_008835.1:g.415697A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8436A>T MANE Select	ENSP00000224721.9:p.Thr2812=
ENST00000642965.1:c.2369A>T	ENSP00000495222.1:n.2369A>T
ENST00000647092.1:c.2033A>T	ENSP00000495176.1:n.2033A>T
ENST00000224721.10:c.8451A>T	ENSP00000224721.8:p.Thr2817=
ENST00000398788.4:c.1716A>T	ENSP00000381768.3:p.Thr572=
ENST00000475158.1:n.1972A>T
ENST00000619887.4:c.1716A>T	ENSP00000478374.1:p.Thr572=
ENST00000622827.4:c.8436A>T	ENSP00000483211.1:p.Thr2812=
NM_001171933.1:c.1716A>T	NP_001165404.1:p.Thr572=
NM_001171934.1:c.1716A>T	NP_001165405.1:p.Thr572=
NM_022124.5:c.8436A>T	NP_071407.4:p.Thr2812=
XM_006717940.2:c.8631A>T	XP_006718003.1:p.Thr2877=
XM_006717942.2:c.8565A>T	XP_006718005.1:p.Thr2855=
XM_011540039.1:c.8628A>T	XP_011538341.1:p.Thr2876=
XM_011540040.1:c.8625A>T	XP_011538342.1:p.Thr2875=
XM_011540041.1:c.8571A>T	XP_011538343.1:p.Thr2857=
XM_011540042.1:c.8541A>T	XP_011538344.1:p.Thr2847=
XM_011540043.1:c.8631A>T	XP_011538345.1:p.Thr2877=
XM_011540044.1:c.8496A>T	XP_011538346.1:p.Thr2832=
XM_011540045.1:c.8631A>T	XP_011538347.1:p.Thr2877=
XM_011540046.1:c.8091A>T	XP_011538348.1:p.Thr2697=
XM_011540047.1:c.7449A>T	XP_011538349.1:p.Thr2483=
XM_011540052.1:c.4959A>T	XP_011538354.1:p.Thr1653=
NM_022124.6:c.8436A>T MANE Select	NP_071407.4:p.Thr2812=