Canonical Allele Identifier: CA1918840993
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71709197T= , CM000672.2:g.71709197T= GRCh38
NC_000010.10:g.73468954T= , CM000672.1:g.73468954T= GRCh37
NC_000010.9:g.73138960T= NCBI36
NG_008835.1:g.317251T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.3206T= MANE Select ENSP00000224721.9:p.Ile1069=
ENST00000398809.9:c.3206T= ENSP00000381789.5:p.Ile1069=
ENST00000442677.4:c.3206T= ENSP00000388894.3:p.Ile1069=
ENST00000466757.8:c.2637T=
ENST00000224721.10:c.3221T= ENSP00000224721.8:p.Ile1074=
ENST00000398809.8:c.3206T= ENSP00000381789.5:p.Ile1069=
ENST00000442677.3:c.1981T=
ENST00000466757.7:c.2637T=
ENST00000616684.4:c.3206T= ENSP00000482036.2:p.Ile1069=
ENST00000622827.4:c.3206T= ENSP00000483211.1:p.Ile1069=
NM_001171930.1:c.3206T= NP_001165401.1:p.Ile1069=
NM_022124.5:c.3206T= NP_071407.4:p.Ile1069=
XM_006717940.2:c.3401T= XP_006718003.1:p.Ile1134=
XM_006717942.2:c.3335T= XP_006718005.1:p.Ile1112=
XM_011540039.1:c.3401T= XP_011538341.1:p.Ile1134=
XM_011540040.1:c.3395T= XP_011538342.1:p.Ile1132=
XM_011540041.1:c.3341T= XP_011538343.1:p.Ile1114=
XM_011540042.1:c.3401T= XP_011538344.1:p.Ile1134=
XM_011540043.1:c.3401T= XP_011538345.1:p.Ile1134=
XM_011540044.1:c.3266T= XP_011538346.1:p.Ile1089=
XM_011540045.1:c.3401T= XP_011538347.1:p.Ile1134=
XM_011540046.1:c.2861T= XP_011538348.1:p.Ile954=
XM_011540047.1:c.2219T= XP_011538349.1:p.Ile740=
XM_011540048.1:c.3401T= XP_011538350.1:p.Ile1134=
XM_011540049.1:c.3401T= XP_011538351.1:p.Ile1134=
XM_011540050.1:c.3401T= XP_011538352.1:p.Ile1134=
XM_011540051.1:c.3401T= XP_011538353.1:p.Ile1134=
XM_011540053.1:c.3401T= XP_011538355.1:p.Ile1134=
XR_945796.1:n.3644T=
NM_001171930.2:c.3206T= NP_001165401.1:p.Ile1069=
NM_022124.6:c.3206T= MANE Select NP_071407.4:p.Ile1069=