Canonical Allele Identifier: CA1918809291
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71645949A= , CM000672.2:g.71645949A= GRCh38
NC_000010.10:g.73405706A= , CM000672.1:g.73405706A= GRCh37
NC_000010.9:g.73075712A= NCBI36
NG_008835.1:g.254003A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.1259A= MANE Select ENSP00000224721.9:p.Asp420=
ENST00000398809.9:c.1259A= ENSP00000381789.5:p.Asp420=
ENST00000442677.4:c.1259A= ENSP00000388894.3:p.Asp420=
ENST00000466757.8:c.690A=
ENST00000643732.1:n.1095A=
ENST00000646131.1:c.923A= ENSP00000495098.1:p.Asp308=
ENST00000224721.10:c.1274A= ENSP00000224721.8:p.Asp425=
ENST00000299366.11:c.1259A= ENSP00000299366.8:p.Asp420=
ENST00000398809.8:c.1259A= ENSP00000381789.5:p.Asp420=
ENST00000398842.7:c.1004A= ENSP00000381822.4:p.Asp335=
ENST00000442677.3:c.34A=
ENST00000461841.7:c.1259A= ENSP00000473454.2:p.Asp420=
ENST00000466757.7:c.690A=
ENST00000470494.5:c.228A=
ENST00000616684.4:c.1259A= ENSP00000482036.2:p.Asp420=
ENST00000622827.4:c.1259A= ENSP00000483211.1:p.Asp420=
NM_001171930.1:c.1259A= NP_001165401.1:p.Asp420=
NM_001171931.1:c.1259A= NP_001165402.1:p.Asp420=
NM_022124.5:c.1259A= NP_071407.4:p.Asp420=
NM_052836.3:c.1259A= NP_443068.1:p.Asp420=
XM_006717940.2:c.1454A= XP_006718003.1:p.Asp485=
XM_006717942.2:c.1388A= XP_006718005.1:p.Asp463=
XM_011540039.1:c.1454A= XP_011538341.1:p.Asp485=
XM_011540040.1:c.1448A= XP_011538342.1:p.Asp483=
XM_011540041.1:c.1394A= XP_011538343.1:p.Asp465=
XM_011540042.1:c.1454A= XP_011538344.1:p.Asp485=
XM_011540043.1:c.1454A= XP_011538345.1:p.Asp485=
XM_011540044.1:c.1319A= XP_011538346.1:p.Asp440=
XM_011540045.1:c.1454A= XP_011538347.1:p.Asp485=
XM_011540046.1:c.914A= XP_011538348.1:p.Asp305=
XM_011540047.1:c.272A= XP_011538349.1:p.Asp91=
XM_011540048.1:c.1454A= XP_011538350.1:p.Asp485=
XM_011540049.1:c.1454A= XP_011538351.1:p.Asp485=
XM_011540050.1:c.1454A= XP_011538352.1:p.Asp485=
XM_011540051.1:c.1454A= XP_011538353.1:p.Asp485=
XM_011540053.1:c.1454A= XP_011538355.1:p.Asp485=
XM_011540054.1:c.1394A= XP_011538356.1:p.Asp465=
XR_945796.1:n.1697A=
NM_001171930.2:c.1259A= NP_001165401.1:p.Asp420=
NM_001171931.2:c.1259A= NP_001165402.1:p.Asp420=
NM_022124.6:c.1259A= MANE Select NP_071407.4:p.Asp420=
NM_052836.4:c.1259A= NP_443068.1:p.Asp420=