Canonical Allele Identifier: CA377158253

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558280C>G (hg19) ; chr10:g.71798523C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798523C>G , CM000672.2:g.71798523C>G	GRCh38
NC_000010.10:g.73558280C>G , CM000672.1:g.73558280C>G	GRCh37
NC_000010.9:g.73228286C>G	NCBI36
NG_008835.1:g.406577C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6999C>G MANE Select	ENSP00000224721.9:p.Tyr2333Ter
ENST00000642965.1:c.932C>G	ENSP00000495222.1:n.932C>G
ENST00000647092.1:c.596C>G	ENSP00000495176.1:n.596C>G
ENST00000224721.10:c.7014C>G	ENSP00000224721.8:p.Tyr2338Ter
ENST00000398788.4:c.279C>G	ENSP00000381768.3:p.Tyr93Ter
ENST00000475158.1:n.535C>G
ENST00000619887.4:c.279C>G	ENSP00000478374.1:p.Tyr93Ter
ENST00000622827.4:c.6999C>G	ENSP00000483211.1:p.Tyr2333Ter
NM_001171933.1:c.279C>G	NP_001165404.1:p.Tyr93Ter
NM_001171934.1:c.279C>G	NP_001165405.1:p.Tyr93Ter
NM_022124.5:c.6999C>G	NP_071407.4:p.Tyr2333Ter
XM_006717940.2:c.7194C>G	XP_006718003.1:p.Tyr2398Ter
XM_006717942.2:c.7128C>G	XP_006718005.1:p.Tyr2376Ter
XM_011540039.1:c.7191C>G	XP_011538341.1:p.Tyr2397Ter
XM_011540040.1:c.7188C>G	XP_011538342.1:p.Tyr2396Ter
XM_011540041.1:c.7134C>G	XP_011538343.1:p.Tyr2378Ter
XM_011540042.1:c.7104C>G	XP_011538344.1:p.Tyr2368Ter
XM_011540043.1:c.7194C>G	XP_011538345.1:p.Tyr2398Ter
XM_011540044.1:c.7059C>G	XP_011538346.1:p.Tyr2353Ter
XM_011540045.1:c.7194C>G	XP_011538347.1:p.Tyr2398Ter
XM_011540046.1:c.6654C>G	XP_011538348.1:p.Tyr2218Ter
XM_011540047.1:c.6012C>G	XP_011538349.1:p.Tyr2004Ter
XM_011540052.1:c.3522C>G	XP_011538354.1:p.Tyr1174Ter
NM_022124.6:c.6999C>G MANE Select	NP_071407.4:p.Tyr2333Ter