Canonical Allele Identifier: CA470062485

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73562741G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71802984G>T , CM000672.2:g.71802984G>T	GRCh38
NC_000010.10:g.73562741G>T , CM000672.1:g.73562741G>T	GRCh37
NC_000010.9:g.73232747G>T	NCBI36
NG_008835.1:g.411038G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7569G>T MANE Select	ENSP00000224721.9:p.Pro2523=
ENST00000642965.1:c.1502G>T	ENSP00000495222.1:n.1502G>T
ENST00000647092.1:c.1166G>T	ENSP00000495176.1:n.1166G>T
ENST00000224721.10:c.7584G>T	ENSP00000224721.8:p.Pro2528=
ENST00000398788.4:c.849G>T	ENSP00000381768.3:p.Pro283=
ENST00000475158.1:n.1105G>T
ENST00000619887.4:c.849G>T	ENSP00000478374.1:p.Pro283=
ENST00000622827.4:c.7569G>T	ENSP00000483211.1:p.Pro2523=
NM_001171933.1:c.849G>T	NP_001165404.1:p.Pro283=
NM_001171934.1:c.849G>T	NP_001165405.1:p.Pro283=
NM_022124.5:c.7569G>T	NP_071407.4:p.Pro2523=
XM_006717940.2:c.7764G>T	XP_006718003.1:p.Pro2588=
XM_006717942.2:c.7698G>T	XP_006718005.1:p.Pro2566=
XM_011540039.1:c.7761G>T	XP_011538341.1:p.Pro2587=
XM_011540040.1:c.7758G>T	XP_011538342.1:p.Pro2586=
XM_011540041.1:c.7704G>T	XP_011538343.1:p.Pro2568=
XM_011540042.1:c.7674G>T	XP_011538344.1:p.Pro2558=
XM_011540043.1:c.7764G>T	XP_011538345.1:p.Pro2588=
XM_011540044.1:c.7629G>T	XP_011538346.1:p.Pro2543=
XM_011540045.1:c.7764G>T	XP_011538347.1:p.Pro2588=
XM_011540046.1:c.7224G>T	XP_011538348.1:p.Pro2408=
XM_011540047.1:c.6582G>T	XP_011538349.1:p.Pro2194=
XM_011540052.1:c.4092G>T	XP_011538354.1:p.Pro1364=
NM_022124.6:c.7569G>T MANE Select	NP_071407.4:p.Pro2523=