Canonical Allele Identifier: CA470061957

Gene: CDH23

Linked Data

• dbSNP Id: rs2132965452
• MyVariant Identifiers: chr10:g.73558139C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798382C>G , CM000672.2:g.71798382C>G	GRCh38
NC_000010.10:g.73558139C>G , CM000672.1:g.73558139C>G	GRCh37
NC_000010.9:g.73228145C>G	NCBI36
NG_008835.1:g.406436C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6858C>G MANE Select	ENSP00000224721.9:p.Val2286=
ENST00000642965.1:c.791C>G	ENSP00000495222.1:n.791C>G
ENST00000647092.1:c.455C>G	ENSP00000495176.1:n.455C>G
ENST00000224721.10:c.6873C>G	ENSP00000224721.8:p.Val2291=
ENST00000398788.4:c.138C>G	ENSP00000381768.3:p.Val46=
ENST00000475158.1:n.394C>G
ENST00000619887.4:c.138C>G	ENSP00000478374.1:p.Val46=
ENST00000622827.4:c.6858C>G	ENSP00000483211.1:p.Val2286=
NM_001171933.1:c.138C>G	NP_001165404.1:p.Val46=
NM_001171934.1:c.138C>G	NP_001165405.1:p.Val46=
NM_022124.5:c.6858C>G	NP_071407.4:p.Val2286=
XM_006717940.2:c.7053C>G	XP_006718003.1:p.Val2351=
XM_006717942.2:c.6987C>G	XP_006718005.1:p.Val2329=
XM_011540039.1:c.7050C>G	XP_011538341.1:p.Val2350=
XM_011540040.1:c.7047C>G	XP_011538342.1:p.Val2349=
XM_011540041.1:c.6993C>G	XP_011538343.1:p.Val2331=
XM_011540042.1:c.6963C>G	XP_011538344.1:p.Val2321=
XM_011540043.1:c.7053C>G	XP_011538345.1:p.Val2351=
XM_011540044.1:c.6918C>G	XP_011538346.1:p.Val2306=
XM_011540045.1:c.7053C>G	XP_011538347.1:p.Val2351=
XM_011540046.1:c.6513C>G	XP_011538348.1:p.Val2171=
XM_011540047.1:c.5871C>G	XP_011538349.1:p.Val1957=
XM_011540052.1:c.3381C>G	XP_011538354.1:p.Val1127=
NM_022124.6:c.6858C>G MANE Select	NP_071407.4:p.Val2286=