Canonical Allele Identifier: CA377162328

Gene: CDH23

Linked Data

• gnomAD v4: 10-71806192-G-T
• MyVariant Identifiers: chr10:g.73565949G>T (hg19) ; chr10:g.71806192G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71806192G>T , CM000672.2:g.71806192G>T	GRCh38
NC_000010.10:g.73565949G>T , CM000672.1:g.73565949G>T	GRCh37
NC_000010.9:g.73235955G>T	NCBI36
NG_008835.1:g.414246G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8089G>T MANE Select	ENSP00000224721.9:p.Gly2697Cys
ENST00000642965.1:c.2022G>T	ENSP00000495222.1:n.2022G>T
ENST00000647092.1:c.1686G>T	ENSP00000495176.1:n.1686G>T
ENST00000224721.10:c.8104G>T	ENSP00000224721.8:p.Gly2702Cys
ENST00000398788.4:c.1369G>T	ENSP00000381768.3:p.Gly457Cys
ENST00000475158.1:n.1625G>T
ENST00000619887.4:c.1369G>T	ENSP00000478374.1:p.Gly457Cys
ENST00000622827.4:c.8089G>T	ENSP00000483211.1:p.Gly2697Cys
NM_001171933.1:c.1369G>T	NP_001165404.1:p.Gly457Cys
NM_001171934.1:c.1369G>T	NP_001165405.1:p.Gly457Cys
NM_022124.5:c.8089G>T	NP_071407.4:p.Gly2697Cys
XM_006717940.2:c.8284G>T	XP_006718003.1:p.Gly2762Cys
XM_006717942.2:c.8218G>T	XP_006718005.1:p.Gly2740Cys
XM_011540039.1:c.8281G>T	XP_011538341.1:p.Gly2761Cys
XM_011540040.1:c.8278G>T	XP_011538342.1:p.Gly2760Cys
XM_011540041.1:c.8224G>T	XP_011538343.1:p.Gly2742Cys
XM_011540042.1:c.8194G>T	XP_011538344.1:p.Gly2732Cys
XM_011540043.1:c.8284G>T	XP_011538345.1:p.Gly2762Cys
XM_011540044.1:c.8149G>T	XP_011538346.1:p.Gly2717Cys
XM_011540045.1:c.8284G>T	XP_011538347.1:p.Gly2762Cys
XM_011540046.1:c.7744G>T	XP_011538348.1:p.Gly2582Cys
XM_011540047.1:c.7102G>T	XP_011538349.1:p.Gly2368Cys
XM_011540052.1:c.4612G>T	XP_011538354.1:p.Gly1538Cys
NM_022124.6:c.8089G>T MANE Select	NP_071407.4:p.Gly2697Cys