Canonical Allele Identifier: CA1918888922
Gene: CDH23 HGNC NCBI

Linked Data

dbSNP Id: rs1589436734

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71809771T>G , CM000672.2:g.71809771T>G GRCh38
NC_000010.10:g.73569528T>G , CM000672.1:g.73569528T>G GRCh37
NC_000010.9:g.73239534T>G NCBI36
NG_008835.1:g.417825T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.8723-49T>G MANE Select ENSP00000224721.9:n.8723-49T>G
ENST00000642965.1:c.2656-49T>G ENSP00000495222.1:n.2656-49T>G
ENST00000647092.1:c.2320-49T>G ENSP00000495176.1:n.2320-49T>G
ENST00000224721.10:c.8738-49T>G ENSP00000224721.8:n.8738-49T>G
ENST00000398788.4:c.2003-49T>G ENSP00000381768.3:n.2003-49T>G
ENST00000475158.1:n.2259-49T>G
ENST00000619887.4:c.2003-49T>G ENSP00000478374.1:n.2003-49T>G
ENST00000622827.4:c.8723-49T>G ENSP00000483211.1:n.8723-49T>G
NM_001171933.1:c.2003-49T>G NP_001165404.1:n.2003-49T>G
NM_001171934.1:c.2003-49T>G NP_001165405.1:n.2003-49T>G
NM_022124.5:c.8723-49T>G NP_071407.4:n.8723-49T>G
XM_006717940.2:c.8918-49T>G XP_006718003.1:n.8918-49T>G
XM_006717942.2:c.8852-49T>G XP_006718005.1:n.8852-49T>G
XM_011540039.1:c.8915-49T>G XP_011538341.1:n.8915-49T>G
XM_011540040.1:c.8912-49T>G XP_011538342.1:n.8912-49T>G
XM_011540041.1:c.8858-49T>G XP_011538343.1:n.8858-49T>G
XM_011540042.1:c.8828-49T>G XP_011538344.1:n.8828-49T>G
XM_011540043.1:c.8918-49T>G XP_011538345.1:n.8918-49T>G
XM_011540044.1:c.8783-49T>G XP_011538346.1:n.8783-49T>G
XM_011540045.1:c.8918-49T>G XP_011538347.1:n.8918-49T>G
XM_011540046.1:c.8378-49T>G XP_011538348.1:n.8378-49T>G
XM_011540047.1:c.7736-49T>G XP_011538349.1:n.7736-49T>G
XM_011540052.1:c.5246-49T>G XP_011538354.1:n.5246-49T>G
NM_022124.6:c.8723-49T>G MANE Select NP_071407.4:n.8723-49T>G