Canonical Allele Identifier: CA377159976

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73560475G>T (hg19) ; chr10:g.71800718G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800718G>T , CM000672.2:g.71800718G>T	GRCh38
NC_000010.10:g.73560475G>T , CM000672.1:g.73560475G>T	GRCh37
NC_000010.9:g.73230481G>T	NCBI36
NG_008835.1:g.408772G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7445G>T MANE Select	ENSP00000224721.9:p.Gly2482Val
ENST00000642965.1:c.1378G>T	ENSP00000495222.1:n.1378G>T
ENST00000647092.1:c.1042G>T	ENSP00000495176.1:n.1042G>T
ENST00000224721.10:c.7460G>T	ENSP00000224721.8:p.Gly2487Val
ENST00000398788.4:c.725G>T	ENSP00000381768.3:p.Gly242Val
ENST00000475158.1:n.981G>T
ENST00000619887.4:c.725G>T	ENSP00000478374.1:p.Gly242Val
ENST00000622827.4:c.7445G>T	ENSP00000483211.1:p.Gly2482Val
NM_001171933.1:c.725G>T	NP_001165404.1:p.Gly242Val
NM_001171934.1:c.725G>T	NP_001165405.1:p.Gly242Val
NM_022124.5:c.7445G>T	NP_071407.4:p.Gly2482Val
XM_006717940.2:c.7640G>T	XP_006718003.1:p.Gly2547Val
XM_006717942.2:c.7574G>T	XP_006718005.1:p.Gly2525Val
XM_011540039.1:c.7637G>T	XP_011538341.1:p.Gly2546Val
XM_011540040.1:c.7634G>T	XP_011538342.1:p.Gly2545Val
XM_011540041.1:c.7580G>T	XP_011538343.1:p.Gly2527Val
XM_011540042.1:c.7550G>T	XP_011538344.1:p.Gly2517Val
XM_011540043.1:c.7640G>T	XP_011538345.1:p.Gly2547Val
XM_011540044.1:c.7505G>T	XP_011538346.1:p.Gly2502Val
XM_011540045.1:c.7640G>T	XP_011538347.1:p.Gly2547Val
XM_011540046.1:c.7100G>T	XP_011538348.1:p.Gly2367Val
XM_011540047.1:c.6458G>T	XP_011538349.1:p.Gly2153Val
XM_011540052.1:c.3968G>T	XP_011538354.1:p.Gly1323Val
NM_022124.6:c.7445G>T MANE Select	NP_071407.4:p.Gly2482Val