Canonical Allele Identifier: CA377158243

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558278T>A (hg19) ; chr10:g.71798521T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798521T>A , CM000672.2:g.71798521T>A	GRCh38
NC_000010.10:g.73558278T>A , CM000672.1:g.73558278T>A	GRCh37
NC_000010.9:g.73228284T>A	NCBI36
NG_008835.1:g.406575T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6997T>A MANE Select	ENSP00000224721.9:p.Tyr2333Asn
ENST00000642965.1:c.930T>A	ENSP00000495222.1:n.930T>A
ENST00000647092.1:c.594T>A	ENSP00000495176.1:n.594T>A
ENST00000224721.10:c.7012T>A	ENSP00000224721.8:p.Tyr2338Asn
ENST00000398788.4:c.277T>A	ENSP00000381768.3:p.Tyr93Asn
ENST00000475158.1:n.533T>A
ENST00000619887.4:c.277T>A	ENSP00000478374.1:p.Tyr93Asn
ENST00000622827.4:c.6997T>A	ENSP00000483211.1:p.Tyr2333Asn
NM_001171933.1:c.277T>A	NP_001165404.1:p.Tyr93Asn
NM_001171934.1:c.277T>A	NP_001165405.1:p.Tyr93Asn
NM_022124.5:c.6997T>A	NP_071407.4:p.Tyr2333Asn
XM_006717940.2:c.7192T>A	XP_006718003.1:p.Tyr2398Asn
XM_006717942.2:c.7126T>A	XP_006718005.1:p.Tyr2376Asn
XM_011540039.1:c.7189T>A	XP_011538341.1:p.Tyr2397Asn
XM_011540040.1:c.7186T>A	XP_011538342.1:p.Tyr2396Asn
XM_011540041.1:c.7132T>A	XP_011538343.1:p.Tyr2378Asn
XM_011540042.1:c.7102T>A	XP_011538344.1:p.Tyr2368Asn
XM_011540043.1:c.7192T>A	XP_011538345.1:p.Tyr2398Asn
XM_011540044.1:c.7057T>A	XP_011538346.1:p.Tyr2353Asn
XM_011540045.1:c.7192T>A	XP_011538347.1:p.Tyr2398Asn
XM_011540046.1:c.6652T>A	XP_011538348.1:p.Tyr2218Asn
XM_011540047.1:c.6010T>A	XP_011538349.1:p.Tyr2004Asn
XM_011540052.1:c.3520T>A	XP_011538354.1:p.Tyr1174Asn
NM_022124.6:c.6997T>A MANE Select	NP_071407.4:p.Tyr2333Asn