Canonical Allele Identifier: CA377157850
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71798422T>G , CM000672.2:g.71798422T>G GRCh38
NC_000010.10:g.73558179T>G , CM000672.1:g.73558179T>G GRCh37
NC_000010.9:g.73228185T>G NCBI36
NG_008835.1:g.406476T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.6898T>G MANE Select ENSP00000224721.9:p.Tyr2300Asp
ENST00000642965.1:c.831T>G ENSP00000495222.1:n.831T>G
ENST00000647092.1:c.495T>G ENSP00000495176.1:n.495T>G
ENST00000224721.10:c.6913T>G ENSP00000224721.8:p.Tyr2305Asp
ENST00000398788.4:c.178T>G ENSP00000381768.3:p.Tyr60Asp
ENST00000475158.1:n.434T>G
ENST00000619887.4:c.178T>G ENSP00000478374.1:p.Tyr60Asp
ENST00000622827.4:c.6898T>G ENSP00000483211.1:p.Tyr2300Asp
NM_001171933.1:c.178T>G NP_001165404.1:p.Tyr60Asp
NM_001171934.1:c.178T>G NP_001165405.1:p.Tyr60Asp
NM_022124.5:c.6898T>G NP_071407.4:p.Tyr2300Asp
XM_006717940.2:c.7093T>G XP_006718003.1:p.Tyr2365Asp
XM_006717942.2:c.7027T>G XP_006718005.1:p.Tyr2343Asp
XM_011540039.1:c.7090T>G XP_011538341.1:p.Tyr2364Asp
XM_011540040.1:c.7087T>G XP_011538342.1:p.Tyr2363Asp
XM_011540041.1:c.7033T>G XP_011538343.1:p.Tyr2345Asp
XM_011540042.1:c.7003T>G XP_011538344.1:p.Tyr2335Asp
XM_011540043.1:c.7093T>G XP_011538345.1:p.Tyr2365Asp
XM_011540044.1:c.6958T>G XP_011538346.1:p.Tyr2320Asp
XM_011540045.1:c.7093T>G XP_011538347.1:p.Tyr2365Asp
XM_011540046.1:c.6553T>G XP_011538348.1:p.Tyr2185Asp
XM_011540047.1:c.5911T>G XP_011538349.1:p.Tyr1971Asp
XM_011540052.1:c.3421T>G XP_011538354.1:p.Tyr1141Asp
NM_022124.6:c.6898T>G MANE Select NP_071407.4:p.Tyr2300Asp