Canonical Allele Identifier: CA377162329

Gene: CDH23

Linked Data

• gnomAD v4: 10-71806193-G-T
• MyVariant Identifiers: chr10:g.73565950G>T (hg19) ; chr10:g.71806193G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71806193G>T , CM000672.2:g.71806193G>T	GRCh38
NC_000010.10:g.73565950G>T , CM000672.1:g.73565950G>T	GRCh37
NC_000010.9:g.73235956G>T	NCBI36
NG_008835.1:g.414247G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8090G>T MANE Select	ENSP00000224721.9:p.Gly2697Val
ENST00000642965.1:c.2023G>T	ENSP00000495222.1:n.2023G>T
ENST00000647092.1:c.1687G>T	ENSP00000495176.1:n.1687G>T
ENST00000224721.10:c.8105G>T	ENSP00000224721.8:p.Gly2702Val
ENST00000398788.4:c.1370G>T	ENSP00000381768.3:p.Gly457Val
ENST00000475158.1:n.1626G>T
ENST00000619887.4:c.1370G>T	ENSP00000478374.1:p.Gly457Val
ENST00000622827.4:c.8090G>T	ENSP00000483211.1:p.Gly2697Val
NM_001171933.1:c.1370G>T	NP_001165404.1:p.Gly457Val
NM_001171934.1:c.1370G>T	NP_001165405.1:p.Gly457Val
NM_022124.5:c.8090G>T	NP_071407.4:p.Gly2697Val
XM_006717940.2:c.8285G>T	XP_006718003.1:p.Gly2762Val
XM_006717942.2:c.8219G>T	XP_006718005.1:p.Gly2740Val
XM_011540039.1:c.8282G>T	XP_011538341.1:p.Gly2761Val
XM_011540040.1:c.8279G>T	XP_011538342.1:p.Gly2760Val
XM_011540041.1:c.8225G>T	XP_011538343.1:p.Gly2742Val
XM_011540042.1:c.8195G>T	XP_011538344.1:p.Gly2732Val
XM_011540043.1:c.8285G>T	XP_011538345.1:p.Gly2762Val
XM_011540044.1:c.8150G>T	XP_011538346.1:p.Gly2717Val
XM_011540045.1:c.8285G>T	XP_011538347.1:p.Gly2762Val
XM_011540046.1:c.7745G>T	XP_011538348.1:p.Gly2582Val
XM_011540047.1:c.7103G>T	XP_011538349.1:p.Gly2368Val
XM_011540052.1:c.4613G>T	XP_011538354.1:p.Gly1538Val
NM_022124.6:c.8090G>T MANE Select	NP_071407.4:p.Gly2697Val