Canonical Allele Identifier: CA1918809218
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71645795C= , CM000672.2:g.71645795C= GRCh38
NC_000010.10:g.73405552C= , CM000672.1:g.73405552C= GRCh37
NC_000010.9:g.73075558C= NCBI36
NG_008835.1:g.253849C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.1141-36C= MANE Select ENSP00000224721.9:n.1141-36C=
ENST00000398809.9:c.1141-36C= ENSP00000381789.5:n.1141-36C=
ENST00000442677.4:c.1141-36C= ENSP00000388894.3:n.1141-36C=
ENST00000466757.8:c.572-36C=
ENST00000643732.1:n.977-36C=
ENST00000646131.1:c.805-36C= ENSP00000495098.1:n.805-36C=
ENST00000224721.10:c.1156-36C= ENSP00000224721.8:n.1156-36C=
ENST00000299366.11:c.1141-36C= ENSP00000299366.8:n.1141-36C=
ENST00000398809.8:c.1141-36C= ENSP00000381789.5:n.1141-36C=
ENST00000398842.7:c.886-36C= ENSP00000381822.4:n.886-36C=
ENST00000461841.7:c.1141-36C= ENSP00000473454.2:n.1141-36C=
ENST00000466757.7:c.572-36C=
ENST00000470494.5:c.110-36C=
ENST00000616684.4:c.1141-36C= ENSP00000482036.2:n.1141-36C=
ENST00000622827.4:c.1135-30C= ENSP00000483211.1:n.1135-30C=
NM_001171930.1:c.1141-36C= NP_001165401.1:n.1141-36C=
NM_001171931.1:c.1141-36C= NP_001165402.1:n.1141-36C=
NM_022124.5:c.1141-36C= NP_071407.4:n.1141-36C=
NM_052836.3:c.1141-36C= NP_443068.1:n.1141-36C=
XM_006717940.2:c.1336-36C= XP_006718003.1:n.1336-36C=
XM_006717942.2:c.1270-36C= XP_006718005.1:n.1270-36C=
XM_011540039.1:c.1336-36C= XP_011538341.1:n.1336-36C=
XM_011540040.1:c.1330-36C= XP_011538342.1:n.1330-36C=
XM_011540041.1:c.1276-36C= XP_011538343.1:n.1276-36C=
XM_011540042.1:c.1336-36C= XP_011538344.1:n.1336-36C=
XM_011540043.1:c.1336-36C= XP_011538345.1:n.1336-36C=
XM_011540044.1:c.1201-36C= XP_011538346.1:n.1201-36C=
XM_011540045.1:c.1336-36C= XP_011538347.1:n.1336-36C=
XM_011540046.1:c.796-36C= XP_011538348.1:n.796-36C=
XM_011540047.1:c.154-36C= XP_011538349.1:n.154-36C=
XM_011540048.1:c.1336-36C= XP_011538350.1:n.1336-36C=
XM_011540049.1:c.1336-36C= XP_011538351.1:n.1336-36C=
XM_011540050.1:c.1336-36C= XP_011538352.1:n.1336-36C=
XM_011540051.1:c.1336-36C= XP_011538353.1:n.1336-36C=
XM_011540053.1:c.1336-36C= XP_011538355.1:n.1336-36C=
XM_011540054.1:c.1276-36C= XP_011538356.1:n.1276-36C=
XR_945796.1:n.1579-36C=
NM_001171930.2:c.1141-36C= NP_001165401.1:n.1141-36C=
NM_001171931.2:c.1141-36C= NP_001165402.1:n.1141-36C=
NM_022124.6:c.1141-36C= MANE Select NP_071407.4:n.1141-36C=
NM_052836.4:c.1141-36C= NP_443068.1:n.1141-36C=