Canonical Allele Identifier: CA377159292

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73559292C>G (hg19) ; chr10:g.71799535C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799535C>G , CM000672.2:g.71799535C>G	GRCh38
NC_000010.10:g.73559292C>G , CM000672.1:g.73559292C>G	GRCh37
NC_000010.9:g.73229298C>G	NCBI36
NG_008835.1:g.407589C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7268C>G MANE Select	ENSP00000224721.9:p.Thr2423Arg
ENST00000642965.1:c.1201C>G	ENSP00000495222.1:n.1201C>G
ENST00000647092.1:c.865C>G	ENSP00000495176.1:n.865C>G
ENST00000224721.10:c.7283C>G	ENSP00000224721.8:p.Thr2428Arg
ENST00000398788.4:c.548C>G	ENSP00000381768.3:p.Thr183Arg
ENST00000475158.1:n.804C>G
ENST00000619887.4:c.548C>G	ENSP00000478374.1:p.Thr183Arg
ENST00000622827.4:c.7268C>G	ENSP00000483211.1:p.Thr2423Arg
NM_001171933.1:c.548C>G	NP_001165404.1:p.Thr183Arg
NM_001171934.1:c.548C>G	NP_001165405.1:p.Thr183Arg
NM_022124.5:c.7268C>G	NP_071407.4:p.Thr2423Arg
XM_006717940.2:c.7463C>G	XP_006718003.1:p.Thr2488Arg
XM_006717942.2:c.7397C>G	XP_006718005.1:p.Thr2466Arg
XM_011540039.1:c.7460C>G	XP_011538341.1:p.Thr2487Arg
XM_011540040.1:c.7457C>G	XP_011538342.1:p.Thr2486Arg
XM_011540041.1:c.7403C>G	XP_011538343.1:p.Thr2468Arg
XM_011540042.1:c.7373C>G	XP_011538344.1:p.Thr2458Arg
XM_011540043.1:c.7463C>G	XP_011538345.1:p.Thr2488Arg
XM_011540044.1:c.7328C>G	XP_011538346.1:p.Thr2443Arg
XM_011540045.1:c.7463C>G	XP_011538347.1:p.Thr2488Arg
XM_011540046.1:c.6923C>G	XP_011538348.1:p.Thr2308Arg
XM_011540047.1:c.6281C>G	XP_011538349.1:p.Thr2094Arg
XM_011540052.1:c.3791C>G	XP_011538354.1:p.Thr1264Arg
NM_022124.6:c.7268C>G MANE Select	NP_071407.4:p.Thr2423Arg