Canonical Allele Identifier: CA2609589774
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71799489C>G , CM000672.2:g.71799489C>G GRCh38
NC_000010.10:g.73559246C>G , CM000672.1:g.73559246C>G GRCh37
NC_000010.9:g.73229252C>G NCBI36
NG_008835.1:g.407543C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.7225-3C>G MANE Select ENSP00000224721.9:n.7225-3C>G
ENST00000642965.1:c.1158-3C>G ENSP00000495222.1:n.1158-3C>G
ENST00000647092.1:c.822-3C>G ENSP00000495176.1:n.822-3C>G
ENST00000224721.10:c.7240-3C>G ENSP00000224721.8:n.7240-3C>G
ENST00000398788.4:c.505-3C>G ENSP00000381768.3:n.505-3C>G
ENST00000475158.1:n.761-3C>G
ENST00000619887.4:c.505-3C>G ENSP00000478374.1:n.505-3C>G
ENST00000622827.4:c.7225-3C>G ENSP00000483211.1:n.7225-3C>G
NM_001171933.1:c.505-3C>G NP_001165404.1:n.505-3C>G
NM_001171934.1:c.505-3C>G NP_001165405.1:n.505-3C>G
NM_022124.5:c.7225-3C>G NP_071407.4:n.7225-3C>G
XM_006717940.2:c.7420-3C>G XP_006718003.1:n.7420-3C>G
XM_006717942.2:c.7354-3C>G XP_006718005.1:n.7354-3C>G
XM_011540039.1:c.7417-3C>G XP_011538341.1:n.7417-3C>G
XM_011540040.1:c.7414-3C>G XP_011538342.1:n.7414-3C>G
XM_011540041.1:c.7360-3C>G XP_011538343.1:n.7360-3C>G
XM_011540042.1:c.7330-3C>G XP_011538344.1:n.7330-3C>G
XM_011540043.1:c.7420-3C>G XP_011538345.1:n.7420-3C>G
XM_011540044.1:c.7285-3C>G XP_011538346.1:n.7285-3C>G
XM_011540045.1:c.7420-3C>G XP_011538347.1:n.7420-3C>G
XM_011540046.1:c.6880-3C>G XP_011538348.1:n.6880-3C>G
XM_011540047.1:c.6238-3C>G XP_011538349.1:n.6238-3C>G
XM_011540052.1:c.3748-3C>G XP_011538354.1:n.3748-3C>G
NM_022124.6:c.7225-3C>G MANE Select NP_071407.4:n.7225-3C>G