Canonical Allele Identifier: CA377158250

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558279A>G (hg19) ; chr10:g.71798522A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798522A>G , CM000672.2:g.71798522A>G	GRCh38
NC_000010.10:g.73558279A>G , CM000672.1:g.73558279A>G	GRCh37
NC_000010.9:g.73228285A>G	NCBI36
NG_008835.1:g.406576A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6998A>G MANE Select	ENSP00000224721.9:p.Tyr2333Cys
ENST00000642965.1:c.931A>G	ENSP00000495222.1:n.931A>G
ENST00000647092.1:c.595A>G	ENSP00000495176.1:n.595A>G
ENST00000224721.10:c.7013A>G	ENSP00000224721.8:p.Tyr2338Cys
ENST00000398788.4:c.278A>G	ENSP00000381768.3:p.Tyr93Cys
ENST00000475158.1:n.534A>G
ENST00000619887.4:c.278A>G	ENSP00000478374.1:p.Tyr93Cys
ENST00000622827.4:c.6998A>G	ENSP00000483211.1:p.Tyr2333Cys
NM_001171933.1:c.278A>G	NP_001165404.1:p.Tyr93Cys
NM_001171934.1:c.278A>G	NP_001165405.1:p.Tyr93Cys
NM_022124.5:c.6998A>G	NP_071407.4:p.Tyr2333Cys
XM_006717940.2:c.7193A>G	XP_006718003.1:p.Tyr2398Cys
XM_006717942.2:c.7127A>G	XP_006718005.1:p.Tyr2376Cys
XM_011540039.1:c.7190A>G	XP_011538341.1:p.Tyr2397Cys
XM_011540040.1:c.7187A>G	XP_011538342.1:p.Tyr2396Cys
XM_011540041.1:c.7133A>G	XP_011538343.1:p.Tyr2378Cys
XM_011540042.1:c.7103A>G	XP_011538344.1:p.Tyr2368Cys
XM_011540043.1:c.7193A>G	XP_011538345.1:p.Tyr2398Cys
XM_011540044.1:c.7058A>G	XP_011538346.1:p.Tyr2353Cys
XM_011540045.1:c.7193A>G	XP_011538347.1:p.Tyr2398Cys
XM_011540046.1:c.6653A>G	XP_011538348.1:p.Tyr2218Cys
XM_011540047.1:c.6011A>G	XP_011538349.1:p.Tyr2004Cys
XM_011540052.1:c.3521A>G	XP_011538354.1:p.Tyr1174Cys
NM_022124.6:c.6998A>G MANE Select	NP_071407.4:p.Tyr2333Cys