Canonical Allele Identifier: CA668097417
Gene: CDH23 HGNC NCBI

Linked Data

dbSNP Id: rs1171434861

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71740757A>T , CM000672.2:g.71740757A>T GRCh38
NC_000010.10:g.73500514A>T , CM000672.1:g.73500514A>T GRCh37
NC_000010.9:g.73170520A>T NCBI36
NG_008835.1:g.348811A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.4489-65A>T MANE Select ENSP00000224721.9:n.4489-65A>T
ENST00000224721.10:c.4504-65A>T ENSP00000224721.8:n.4504-65A>T
ENST00000398792.3:n.1178-65A>T
ENST00000622827.4:c.4489-65A>T ENSP00000483211.1:n.4489-65A>T
NM_022124.5:c.4489-65A>T NP_071407.4:n.4489-65A>T
XM_006717940.2:c.4684-65A>T XP_006718003.1:n.4684-65A>T
XM_006717942.2:c.4618-65A>T XP_006718005.1:n.4618-65A>T
XM_011540039.1:c.4681-65A>T XP_011538341.1:n.4681-65A>T
XM_011540040.1:c.4678-65A>T XP_011538342.1:n.4678-65A>T
XM_011540041.1:c.4624-65A>T XP_011538343.1:n.4624-65A>T
XM_011540042.1:c.4684-65A>T XP_011538344.1:n.4684-65A>T
XM_011540043.1:c.4684-65A>T XP_011538345.1:n.4684-65A>T
XM_011540044.1:c.4549-65A>T XP_011538346.1:n.4549-65A>T
XM_011540045.1:c.4684-65A>T XP_011538347.1:n.4684-65A>T
XM_011540046.1:c.4144-65A>T XP_011538348.1:n.4144-65A>T
XM_011540047.1:c.3502-65A>T XP_011538349.1:n.3502-65A>T
XM_011540048.1:c.4684-65A>T XP_011538350.1:n.4684-65A>T
XM_011540049.1:c.4684-65A>T XP_011538351.1:n.4684-65A>T
XM_011540050.1:c.4684-65A>T XP_011538352.1:n.4684-65A>T
XM_011540051.1:c.4684-65A>T XP_011538353.1:n.4684-65A>T
XM_011540052.1:c.1012-65A>T XP_011538354.1:n.1012-65A>T
XM_011540053.1:c.4684-65A>T XP_011538355.1:n.4684-65A>T
XR_945796.1:n.4927-65A>T
NM_022124.6:c.4489-65A>T MANE Select NP_071407.4:n.4489-65A>T