Canonical Allele Identifier: CA1918840777
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71709122G= , CM000672.2:g.71709122G= GRCh38
NC_000010.10:g.73468879G= , CM000672.1:g.73468879G= GRCh37
NC_000010.9:g.73138885G= NCBI36
NG_008835.1:g.317176G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.3131G= MANE Select ENSP00000224721.9:p.Ser1044=
ENST00000398809.9:c.3131G= ENSP00000381789.5:p.Ser1044=
ENST00000442677.4:c.3131G= ENSP00000388894.3:p.Ser1044=
ENST00000466757.8:c.2562G=
ENST00000224721.10:c.3146G= ENSP00000224721.8:p.Ser1049=
ENST00000398809.8:c.3131G= ENSP00000381789.5:p.Ser1044=
ENST00000442677.3:c.1906G=
ENST00000466757.7:c.2562G=
ENST00000616684.4:c.3131G= ENSP00000482036.2:p.Ser1044=
ENST00000622827.4:c.3131G= ENSP00000483211.1:p.Ser1044=
NM_001171930.1:c.3131G= NP_001165401.1:p.Ser1044=
NM_022124.5:c.3131G= NP_071407.4:p.Ser1044=
XM_006717940.2:c.3326G= XP_006718003.1:p.Ser1109=
XM_006717942.2:c.3260G= XP_006718005.1:p.Ser1087=
XM_011540039.1:c.3326G= XP_011538341.1:p.Ser1109=
XM_011540040.1:c.3320G= XP_011538342.1:p.Ser1107=
XM_011540041.1:c.3266G= XP_011538343.1:p.Ser1089=
XM_011540042.1:c.3326G= XP_011538344.1:p.Ser1109=
XM_011540043.1:c.3326G= XP_011538345.1:p.Ser1109=
XM_011540044.1:c.3191G= XP_011538346.1:p.Ser1064=
XM_011540045.1:c.3326G= XP_011538347.1:p.Ser1109=
XM_011540046.1:c.2786G= XP_011538348.1:p.Ser929=
XM_011540047.1:c.2144G= XP_011538349.1:p.Ser715=
XM_011540048.1:c.3326G= XP_011538350.1:p.Ser1109=
XM_011540049.1:c.3326G= XP_011538351.1:p.Ser1109=
XM_011540050.1:c.3326G= XP_011538352.1:p.Ser1109=
XM_011540051.1:c.3326G= XP_011538353.1:p.Ser1109=
XM_011540053.1:c.3326G= XP_011538355.1:p.Ser1109=
XR_945796.1:n.3569G=
NM_001171930.2:c.3131G= NP_001165401.1:p.Ser1044=
NM_022124.6:c.3131G= MANE Select NP_071407.4:p.Ser1044=