Canonical Allele Identifier: CA377159833

Gene: CDH23

Linked Data

• gnomAD v4: 10-71800649-T-G
• MyVariant Identifiers: chr10:g.73560406T>G (hg19) ; chr10:g.71800649T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800649T>G , CM000672.2:g.71800649T>G	GRCh38
NC_000010.10:g.73560406T>G , CM000672.1:g.73560406T>G	GRCh37
NC_000010.9:g.73230412T>G	NCBI36
NG_008835.1:g.408703T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7376T>G MANE Select	ENSP00000224721.9:p.Val2459Gly
ENST00000642965.1:c.1309T>G	ENSP00000495222.1:n.1309T>G
ENST00000647092.1:c.973T>G	ENSP00000495176.1:n.973T>G
ENST00000224721.10:c.7391T>G	ENSP00000224721.8:p.Val2464Gly
ENST00000398788.4:c.656T>G	ENSP00000381768.3:p.Val219Gly
ENST00000475158.1:n.912T>G
ENST00000619887.4:c.656T>G	ENSP00000478374.1:p.Val219Gly
ENST00000622827.4:c.7376T>G	ENSP00000483211.1:p.Val2459Gly
NM_001171933.1:c.656T>G	NP_001165404.1:p.Val219Gly
NM_001171934.1:c.656T>G	NP_001165405.1:p.Val219Gly
NM_022124.5:c.7376T>G	NP_071407.4:p.Val2459Gly
XM_006717940.2:c.7571T>G	XP_006718003.1:p.Val2524Gly
XM_006717942.2:c.7505T>G	XP_006718005.1:p.Val2502Gly
XM_011540039.1:c.7568T>G	XP_011538341.1:p.Val2523Gly
XM_011540040.1:c.7565T>G	XP_011538342.1:p.Val2522Gly
XM_011540041.1:c.7511T>G	XP_011538343.1:p.Val2504Gly
XM_011540042.1:c.7481T>G	XP_011538344.1:p.Val2494Gly
XM_011540043.1:c.7571T>G	XP_011538345.1:p.Val2524Gly
XM_011540044.1:c.7436T>G	XP_011538346.1:p.Val2479Gly
XM_011540045.1:c.7571T>G	XP_011538347.1:p.Val2524Gly
XM_011540046.1:c.7031T>G	XP_011538348.1:p.Val2344Gly
XM_011540047.1:c.6389T>G	XP_011538349.1:p.Val2130Gly
XM_011540052.1:c.3899T>G	XP_011538354.1:p.Val1300Gly
NM_022124.6:c.7376T>G MANE Select	NP_071407.4:p.Val2459Gly