Canonical Allele Identifier: CA377159818

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73560402T>G (hg19) ; chr10:g.71800645T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800645T>G , CM000672.2:g.71800645T>G	GRCh38
NC_000010.10:g.73560402T>G , CM000672.1:g.73560402T>G	GRCh37
NC_000010.9:g.73230408T>G	NCBI36
NG_008835.1:g.408699T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7372T>G MANE Select	ENSP00000224721.9:p.Tyr2458Asp
ENST00000642965.1:c.1305T>G	ENSP00000495222.1:n.1305T>G
ENST00000647092.1:c.969T>G	ENSP00000495176.1:n.969T>G
ENST00000224721.10:c.7387T>G	ENSP00000224721.8:p.Tyr2463Asp
ENST00000398788.4:c.652T>G	ENSP00000381768.3:p.Tyr218Asp
ENST00000475158.1:n.908T>G
ENST00000619887.4:c.652T>G	ENSP00000478374.1:p.Tyr218Asp
ENST00000622827.4:c.7372T>G	ENSP00000483211.1:p.Tyr2458Asp
NM_001171933.1:c.652T>G	NP_001165404.1:p.Tyr218Asp
NM_001171934.1:c.652T>G	NP_001165405.1:p.Tyr218Asp
NM_022124.5:c.7372T>G	NP_071407.4:p.Tyr2458Asp
XM_006717940.2:c.7567T>G	XP_006718003.1:p.Tyr2523Asp
XM_006717942.2:c.7501T>G	XP_006718005.1:p.Tyr2501Asp
XM_011540039.1:c.7564T>G	XP_011538341.1:p.Tyr2522Asp
XM_011540040.1:c.7561T>G	XP_011538342.1:p.Tyr2521Asp
XM_011540041.1:c.7507T>G	XP_011538343.1:p.Tyr2503Asp
XM_011540042.1:c.7477T>G	XP_011538344.1:p.Tyr2493Asp
XM_011540043.1:c.7567T>G	XP_011538345.1:p.Tyr2523Asp
XM_011540044.1:c.7432T>G	XP_011538346.1:p.Tyr2478Asp
XM_011540045.1:c.7567T>G	XP_011538347.1:p.Tyr2523Asp
XM_011540046.1:c.7027T>G	XP_011538348.1:p.Tyr2343Asp
XM_011540047.1:c.6385T>G	XP_011538349.1:p.Tyr2129Asp
XM_011540052.1:c.3895T>G	XP_011538354.1:p.Tyr1299Asp
NM_022124.6:c.7372T>G MANE Select	NP_071407.4:p.Tyr2458Asp