Canonical Allele Identifier: CA377159300

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73559295T>G (hg19) ; chr10:g.71799538T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799538T>G , CM000672.2:g.71799538T>G	GRCh38
NC_000010.10:g.73559295T>G , CM000672.1:g.73559295T>G	GRCh37
NC_000010.9:g.73229301T>G	NCBI36
NG_008835.1:g.407592T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7271T>G MANE Select	ENSP00000224721.9:p.Val2424Gly
ENST00000642965.1:c.1204T>G	ENSP00000495222.1:n.1204T>G
ENST00000647092.1:c.868T>G	ENSP00000495176.1:n.868T>G
ENST00000224721.10:c.7286T>G	ENSP00000224721.8:p.Val2429Gly
ENST00000398788.4:c.551T>G	ENSP00000381768.3:p.Val184Gly
ENST00000475158.1:n.807T>G
ENST00000619887.4:c.551T>G	ENSP00000478374.1:p.Val184Gly
ENST00000622827.4:c.7271T>G	ENSP00000483211.1:p.Val2424Gly
NM_001171933.1:c.551T>G	NP_001165404.1:p.Val184Gly
NM_001171934.1:c.551T>G	NP_001165405.1:p.Val184Gly
NM_022124.5:c.7271T>G	NP_071407.4:p.Val2424Gly
XM_006717940.2:c.7466T>G	XP_006718003.1:p.Val2489Gly
XM_006717942.2:c.7400T>G	XP_006718005.1:p.Val2467Gly
XM_011540039.1:c.7463T>G	XP_011538341.1:p.Val2488Gly
XM_011540040.1:c.7460T>G	XP_011538342.1:p.Val2487Gly
XM_011540041.1:c.7406T>G	XP_011538343.1:p.Val2469Gly
XM_011540042.1:c.7376T>G	XP_011538344.1:p.Val2459Gly
XM_011540043.1:c.7466T>G	XP_011538345.1:p.Val2489Gly
XM_011540044.1:c.7331T>G	XP_011538346.1:p.Val2444Gly
XM_011540045.1:c.7466T>G	XP_011538347.1:p.Val2489Gly
XM_011540046.1:c.6926T>G	XP_011538348.1:p.Val2309Gly
XM_011540047.1:c.6284T>G	XP_011538349.1:p.Val2095Gly
XM_011540052.1:c.3794T>G	XP_011538354.1:p.Val1265Gly
NM_022124.6:c.7271T>G MANE Select	NP_071407.4:p.Val2424Gly