Canonical Allele Identifier: CA1918840959
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71709180A= , CM000672.2:g.71709180A= GRCh38
NC_000010.10:g.73468937A= , CM000672.1:g.73468937A= GRCh37
NC_000010.9:g.73138943A= NCBI36
NG_008835.1:g.317234A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.3189A= MANE Select ENSP00000224721.9:p.Thr1063=
ENST00000398809.9:c.3189A= ENSP00000381789.5:p.Thr1063=
ENST00000442677.4:c.3189A= ENSP00000388894.3:p.Thr1063=
ENST00000466757.8:c.2620A=
ENST00000224721.10:c.3204A= ENSP00000224721.8:p.Thr1068=
ENST00000398809.8:c.3189A= ENSP00000381789.5:p.Thr1063=
ENST00000442677.3:c.1964A=
ENST00000466757.7:c.2620A=
ENST00000616684.4:c.3189A= ENSP00000482036.2:p.Thr1063=
ENST00000622827.4:c.3189A= ENSP00000483211.1:p.Thr1063=
NM_001171930.1:c.3189A= NP_001165401.1:p.Thr1063=
NM_022124.5:c.3189A= NP_071407.4:p.Thr1063=
XM_006717940.2:c.3384A= XP_006718003.1:p.Thr1128=
XM_006717942.2:c.3318A= XP_006718005.1:p.Thr1106=
XM_011540039.1:c.3384A= XP_011538341.1:p.Thr1128=
XM_011540040.1:c.3378A= XP_011538342.1:p.Thr1126=
XM_011540041.1:c.3324A= XP_011538343.1:p.Thr1108=
XM_011540042.1:c.3384A= XP_011538344.1:p.Thr1128=
XM_011540043.1:c.3384A= XP_011538345.1:p.Thr1128=
XM_011540044.1:c.3249A= XP_011538346.1:p.Thr1083=
XM_011540045.1:c.3384A= XP_011538347.1:p.Thr1128=
XM_011540046.1:c.2844A= XP_011538348.1:p.Thr948=
XM_011540047.1:c.2202A= XP_011538349.1:p.Thr734=
XM_011540048.1:c.3384A= XP_011538350.1:p.Thr1128=
XM_011540049.1:c.3384A= XP_011538351.1:p.Thr1128=
XM_011540050.1:c.3384A= XP_011538352.1:p.Thr1128=
XM_011540051.1:c.3384A= XP_011538353.1:p.Thr1128=
XM_011540053.1:c.3384A= XP_011538355.1:p.Thr1128=
XR_945796.1:n.3627A=
NM_001171930.2:c.3189A= NP_001165401.1:p.Thr1063=
NM_022124.6:c.3189A= MANE Select NP_071407.4:p.Thr1063=