Canonical Allele Identifier: CA377159779

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73560393G>A (hg19) ; chr10:g.71800636G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800636G>A , CM000672.2:g.71800636G>A	GRCh38
NC_000010.10:g.73560393G>A , CM000672.1:g.73560393G>A	GRCh37
NC_000010.9:g.73230399G>A	NCBI36
NG_008835.1:g.408690G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7363G>A MANE Select	ENSP00000224721.9:p.Gly2455Ser
ENST00000642965.1:c.1296G>A	ENSP00000495222.1:n.1296G>A
ENST00000647092.1:c.960G>A	ENSP00000495176.1:n.960G>A
ENST00000224721.10:c.7378G>A	ENSP00000224721.8:p.Gly2460Ser
ENST00000398788.4:c.643G>A	ENSP00000381768.3:p.Gly215Ser
ENST00000475158.1:n.899G>A
ENST00000619887.4:c.643G>A	ENSP00000478374.1:p.Gly215Ser
ENST00000622827.4:c.7363G>A	ENSP00000483211.1:p.Gly2455Ser
NM_001171933.1:c.643G>A	NP_001165404.1:p.Gly215Ser
NM_001171934.1:c.643G>A	NP_001165405.1:p.Gly215Ser
NM_022124.5:c.7363G>A	NP_071407.4:p.Gly2455Ser
XM_006717940.2:c.7558G>A	XP_006718003.1:p.Gly2520Ser
XM_006717942.2:c.7492G>A	XP_006718005.1:p.Gly2498Ser
XM_011540039.1:c.7555G>A	XP_011538341.1:p.Gly2519Ser
XM_011540040.1:c.7552G>A	XP_011538342.1:p.Gly2518Ser
XM_011540041.1:c.7498G>A	XP_011538343.1:p.Gly2500Ser
XM_011540042.1:c.7468G>A	XP_011538344.1:p.Gly2490Ser
XM_011540043.1:c.7558G>A	XP_011538345.1:p.Gly2520Ser
XM_011540044.1:c.7423G>A	XP_011538346.1:p.Gly2475Ser
XM_011540045.1:c.7558G>A	XP_011538347.1:p.Gly2520Ser
XM_011540046.1:c.7018G>A	XP_011538348.1:p.Gly2340Ser
XM_011540047.1:c.6376G>A	XP_011538349.1:p.Gly2126Ser
XM_011540052.1:c.3886G>A	XP_011538354.1:p.Gly1296Ser
NM_022124.6:c.7363G>A MANE Select	NP_071407.4:p.Gly2455Ser