Canonical Allele Identifier: CA1918769765
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71570888C= , CM000672.2:g.71570888C= GRCh38
NC_000010.10:g.73330645C= , CM000672.1:g.73330645C= GRCh37
NC_000010.9:g.73000651C= NCBI36
NG_008835.1:g.178942C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.723C= MANE Select ENSP00000224721.9:p.Tyr241=
ENST00000398809.9:c.723C= ENSP00000381789.5:p.Tyr241=
ENST00000442677.4:c.723C= ENSP00000388894.3:p.Tyr241=
ENST00000466757.8:c.94C=
ENST00000643732.1:n.499C=
ENST00000646131.1:c.387C= ENSP00000495098.1:p.Tyr129=
ENST00000224721.10:c.738C= ENSP00000224721.8:p.Tyr246=
ENST00000299366.11:c.723C= ENSP00000299366.8:p.Tyr241=
ENST00000398809.8:c.723C= ENSP00000381789.5:p.Tyr241=
ENST00000398842.7:c.474C= ENSP00000381822.4:p.Tyr158=
ENST00000461841.7:c.723C= ENSP00000473454.2:p.Tyr241=
ENST00000466757.7:c.94C=
ENST00000616684.4:c.723C= ENSP00000482036.2:p.Tyr241=
ENST00000622827.4:c.723C= ENSP00000483211.1:p.Tyr241=
NM_001171930.1:c.723C= NP_001165401.1:p.Tyr241=
NM_001171931.1:c.723C= NP_001165402.1:p.Tyr241=
NM_001171932.1:c.723C= NP_001165403.1:p.Tyr241=
NM_022124.5:c.723C= NP_071407.4:p.Tyr241=
NM_052836.3:c.723C= NP_443068.1:p.Tyr241=
XM_006717940.2:c.858C= XP_006718003.1:p.Tyr286=
XM_006717942.2:c.858C= XP_006718005.1:p.Tyr286=
XM_011540039.1:c.858C= XP_011538341.1:p.Tyr286=
XM_011540040.1:c.858C= XP_011538342.1:p.Tyr286=
XM_011540041.1:c.858C= XP_011538343.1:p.Tyr286=
XM_011540042.1:c.858C= XP_011538344.1:p.Tyr286=
XM_011540043.1:c.858C= XP_011538345.1:p.Tyr286=
XM_011540044.1:c.723C= XP_011538346.1:p.Tyr241=
XM_011540045.1:c.858C= XP_011538347.1:p.Tyr286=
XM_011540046.1:c.318C= XP_011538348.1:p.Tyr106=
XM_011540048.1:c.858C= XP_011538350.1:p.Tyr286=
XM_011540049.1:c.858C= XP_011538351.1:p.Tyr286=
XM_011540050.1:c.858C= XP_011538352.1:p.Tyr286=
XM_011540051.1:c.858C= XP_011538353.1:p.Tyr286=
XM_011540053.1:c.858C= XP_011538355.1:p.Tyr286=
XM_011540054.1:c.858C= XP_011538356.1:p.Tyr286=
XR_246128.2:n.162-5754G=
XR_945796.1:n.1101C=
NM_001171930.2:c.723C= NP_001165401.1:p.Tyr241=
NM_001171931.2:c.723C= NP_001165402.1:p.Tyr241=
NM_022124.6:c.723C= MANE Select NP_071407.4:p.Tyr241=
NM_052836.4:c.723C= NP_443068.1:p.Tyr241=
NM_001171932.2:c.723C= NP_001165403.1:p.Tyr241=