Canonical Allele Identifier: CA377159140
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71799502T>G , CM000672.2:g.71799502T>G GRCh38
NC_000010.10:g.73559259T>G , CM000672.1:g.73559259T>G GRCh37
NC_000010.9:g.73229265T>G NCBI36
NG_008835.1:g.407556T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.7235T>G MANE Select ENSP00000224721.9:p.Phe2412Cys
ENST00000642965.1:c.1168T>G ENSP00000495222.1:n.1168T>G
ENST00000647092.1:c.832T>G ENSP00000495176.1:n.832T>G
ENST00000224721.10:c.7250T>G ENSP00000224721.8:p.Phe2417Cys
ENST00000398788.4:c.515T>G ENSP00000381768.3:p.Phe172Cys
ENST00000475158.1:n.771T>G
ENST00000619887.4:c.515T>G ENSP00000478374.1:p.Phe172Cys
ENST00000622827.4:c.7235T>G ENSP00000483211.1:p.Phe2412Cys
NM_001171933.1:c.515T>G NP_001165404.1:p.Phe172Cys
NM_001171934.1:c.515T>G NP_001165405.1:p.Phe172Cys
NM_022124.5:c.7235T>G NP_071407.4:p.Phe2412Cys
XM_006717940.2:c.7430T>G XP_006718003.1:p.Phe2477Cys
XM_006717942.2:c.7364T>G XP_006718005.1:p.Phe2455Cys
XM_011540039.1:c.7427T>G XP_011538341.1:p.Phe2476Cys
XM_011540040.1:c.7424T>G XP_011538342.1:p.Phe2475Cys
XM_011540041.1:c.7370T>G XP_011538343.1:p.Phe2457Cys
XM_011540042.1:c.7340T>G XP_011538344.1:p.Phe2447Cys
XM_011540043.1:c.7430T>G XP_011538345.1:p.Phe2477Cys
XM_011540044.1:c.7295T>G XP_011538346.1:p.Phe2432Cys
XM_011540045.1:c.7430T>G XP_011538347.1:p.Phe2477Cys
XM_011540046.1:c.6890T>G XP_011538348.1:p.Phe2297Cys
XM_011540047.1:c.6248T>G XP_011538349.1:p.Phe2083Cys
XM_011540052.1:c.3758T>G XP_011538354.1:p.Phe1253Cys
NM_022124.6:c.7235T>G MANE Select NP_071407.4:p.Phe2412Cys