Canonical Allele Identifier: CA470062295

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73560488C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800731C>T , CM000672.2:g.71800731C>T	GRCh38
NC_000010.10:g.73560488C>T , CM000672.1:g.73560488C>T	GRCh37
NC_000010.9:g.73230494C>T	NCBI36
NG_008835.1:g.408785C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7458C>T MANE Select	ENSP00000224721.9:p.Ser2486=
ENST00000642965.1:c.1391C>T	ENSP00000495222.1:n.1391C>T
ENST00000647092.1:c.1055C>T	ENSP00000495176.1:n.1055C>T
ENST00000224721.10:c.7473C>T	ENSP00000224721.8:p.Ser2491=
ENST00000398788.4:c.738C>T	ENSP00000381768.3:p.Ser246=
ENST00000475158.1:n.994C>T
ENST00000619887.4:c.738C>T	ENSP00000478374.1:p.Ser246=
ENST00000622827.4:c.7458C>T	ENSP00000483211.1:p.Ser2486=
NM_001171933.1:c.738C>T	NP_001165404.1:p.Ser246=
NM_001171934.1:c.738C>T	NP_001165405.1:p.Ser246=
NM_022124.5:c.7458C>T	NP_071407.4:p.Ser2486=
XM_006717940.2:c.7653C>T	XP_006718003.1:p.Ser2551=
XM_006717942.2:c.7587C>T	XP_006718005.1:p.Ser2529=
XM_011540039.1:c.7650C>T	XP_011538341.1:p.Ser2550=
XM_011540040.1:c.7647C>T	XP_011538342.1:p.Ser2549=
XM_011540041.1:c.7593C>T	XP_011538343.1:p.Ser2531=
XM_011540042.1:c.7563C>T	XP_011538344.1:p.Ser2521=
XM_011540043.1:c.7653C>T	XP_011538345.1:p.Ser2551=
XM_011540044.1:c.7518C>T	XP_011538346.1:p.Ser2506=
XM_011540045.1:c.7653C>T	XP_011538347.1:p.Ser2551=
XM_011540046.1:c.7113C>T	XP_011538348.1:p.Ser2371=
XM_011540047.1:c.6471C>T	XP_011538349.1:p.Ser2157=
XM_011540052.1:c.3981C>T	XP_011538354.1:p.Ser1327=
NM_022124.6:c.7458C>T MANE Select	NP_071407.4:p.Ser2486=