Canonical Allele Identifier: CA470282197

Gene: CDH23

Linked Data

• dbSNP Id: rs1318586803
• gnomAD v2: 10-73565951-C-T
• gnomAD v4: 10-71806194-C-T
• MyVariant Identifiers: chr10:g.73565951C>T (hg19) ; chr10:g.71806194C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71806194C>T , CM000672.2:g.71806194C>T	GRCh38
NC_000010.10:g.73565951C>T , CM000672.1:g.73565951C>T	GRCh37
NC_000010.9:g.73235957C>T	NCBI36
NG_008835.1:g.414248C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8091C>T MANE Select	ENSP00000224721.9:p.Gly2697=
ENST00000642965.1:c.2024C>T	ENSP00000495222.1:n.2024C>T
ENST00000647092.1:c.1688C>T	ENSP00000495176.1:n.1688C>T
ENST00000224721.10:c.8106C>T	ENSP00000224721.8:p.Gly2702=
ENST00000398788.4:c.1371C>T	ENSP00000381768.3:p.Gly457=
ENST00000475158.1:n.1627C>T
ENST00000619887.4:c.1371C>T	ENSP00000478374.1:p.Gly457=
ENST00000622827.4:c.8091C>T	ENSP00000483211.1:p.Gly2697=
NM_001171933.1:c.1371C>T	NP_001165404.1:p.Gly457=
NM_001171934.1:c.1371C>T	NP_001165405.1:p.Gly457=
NM_022124.5:c.8091C>T	NP_071407.4:p.Gly2697=
XM_006717940.2:c.8286C>T	XP_006718003.1:p.Gly2762=
XM_006717942.2:c.8220C>T	XP_006718005.1:p.Gly2740=
XM_011540039.1:c.8283C>T	XP_011538341.1:p.Gly2761=
XM_011540040.1:c.8280C>T	XP_011538342.1:p.Gly2760=
XM_011540041.1:c.8226C>T	XP_011538343.1:p.Gly2742=
XM_011540042.1:c.8196C>T	XP_011538344.1:p.Gly2732=
XM_011540043.1:c.8286C>T	XP_011538345.1:p.Gly2762=
XM_011540044.1:c.8151C>T	XP_011538346.1:p.Gly2717=
XM_011540045.1:c.8286C>T	XP_011538347.1:p.Gly2762=
XM_011540046.1:c.7746C>T	XP_011538348.1:p.Gly2582=
XM_011540047.1:c.7104C>T	XP_011538349.1:p.Gly2368=
XM_011540052.1:c.4614C>T	XP_011538354.1:p.Gly1538=
NM_022124.6:c.8091C>T MANE Select	NP_071407.4:p.Gly2697=