Canonical Allele Identifier: CA377160675

Gene: CDH23

Linked Data

• dbSNP Id: rs1317005883
• gnomAD v2: 10-73562746-G-A
• gnomAD v3: 10-71802989-G-A
• gnomAD v4: 10-71802989-G-A
• MyVariant Identifiers: chr10:g.73562746G>A (hg19) ; chr10:g.71802989G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71802989G>A , CM000672.2:g.71802989G>A	GRCh38
NC_000010.10:g.73562746G>A , CM000672.1:g.73562746G>A	GRCh37
NC_000010.9:g.73232752G>A	NCBI36
NG_008835.1:g.411043G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7574G>A MANE Select	ENSP00000224721.9:p.Gly2525Asp
ENST00000642965.1:c.1507G>A	ENSP00000495222.1:n.1507G>A
ENST00000647092.1:c.1171G>A	ENSP00000495176.1:n.1171G>A
ENST00000224721.10:c.7589G>A	ENSP00000224721.8:p.Gly2530Asp
ENST00000398788.4:c.854G>A	ENSP00000381768.3:p.Gly285Asp
ENST00000475158.1:n.1110G>A
ENST00000619887.4:c.854G>A	ENSP00000478374.1:p.Gly285Asp
ENST00000622827.4:c.7574G>A	ENSP00000483211.1:p.Gly2525Asp
NM_001171933.1:c.854G>A	NP_001165404.1:p.Gly285Asp
NM_001171934.1:c.854G>A	NP_001165405.1:p.Gly285Asp
NM_022124.5:c.7574G>A	NP_071407.4:p.Gly2525Asp
XM_006717940.2:c.7769G>A	XP_006718003.1:p.Gly2590Asp
XM_006717942.2:c.7703G>A	XP_006718005.1:p.Gly2568Asp
XM_011540039.1:c.7766G>A	XP_011538341.1:p.Gly2589Asp
XM_011540040.1:c.7763G>A	XP_011538342.1:p.Gly2588Asp
XM_011540041.1:c.7709G>A	XP_011538343.1:p.Gly2570Asp
XM_011540042.1:c.7679G>A	XP_011538344.1:p.Gly2560Asp
XM_011540043.1:c.7769G>A	XP_011538345.1:p.Gly2590Asp
XM_011540044.1:c.7634G>A	XP_011538346.1:p.Gly2545Asp
XM_011540045.1:c.7769G>A	XP_011538347.1:p.Gly2590Asp
XM_011540046.1:c.7229G>A	XP_011538348.1:p.Gly2410Asp
XM_011540047.1:c.6587G>A	XP_011538349.1:p.Gly2196Asp
XM_011540052.1:c.4097G>A	XP_011538354.1:p.Gly1366Asp
NM_022124.6:c.7574G>A MANE Select	NP_071407.4:p.Gly2525Asp