Canonical Allele Identifier: CA1918826407

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71687670_71687671delinsCT , CM000672.2:g.71687670_71687671delinsCT	GRCh38
NC_000010.10:g.73447427_73447428delinsCT , CM000672.1:g.73447427_73447428delinsCT	GRCh37
NC_000010.9:g.73117433_73117434delinsCT	NCBI36
NG_008835.1:g.295724_295725delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.2010_2011delinsCT MANE Select	ENSP00000224721.9:p.Thr670=
ENST00000398809.9:c.2010_2011delinsCT	ENSP00000381789.5:p.Thr670=
ENST00000442677.4:c.2010_2011delinsCT	ENSP00000388894.3:p.Thr670=
ENST00000466757.8:c.1441_1442delinsCT
ENST00000224721.10:c.2025_2026delinsCT	ENSP00000224721.8:p.Thr675=
ENST00000299366.11:c.2010_2011delinsCT	ENSP00000299366.8:p.Thr670=
ENST00000398809.8:c.2010_2011delinsCT	ENSP00000381789.5:p.Thr670=
ENST00000442677.3:c.785_786delinsCT
ENST00000466757.7:c.1441_1442delinsCT
ENST00000616684.4:c.2010_2011delinsCT	ENSP00000482036.2:p.Thr670=
ENST00000622827.4:c.2010_2011delinsCT	ENSP00000483211.1:p.Thr670=
NM_001171930.1:c.2010_2011delinsCT	NP_001165401.1:p.Thr670=
NM_001171931.1:c.2010_2011delinsCT	NP_001165402.1:p.Thr670=
NM_022124.5:c.2010_2011delinsCT	NP_071407.4:p.Thr670=
XM_006717940.2:c.2205_2206delinsCT	XP_006718003.1:p.Thr735=
XM_006717942.2:c.2139_2140delinsCT	XP_006718005.1:p.Thr713=
XM_011540039.1:c.2205_2206delinsCT	XP_011538341.1:p.Thr735=
XM_011540040.1:c.2199_2200delinsCT	XP_011538342.1:p.Thr733=
XM_011540041.1:c.2145_2146delinsCT	XP_011538343.1:p.Thr715=
XM_011540042.1:c.2205_2206delinsCT	XP_011538344.1:p.Thr735=
XM_011540043.1:c.2205_2206delinsCT	XP_011538345.1:p.Thr735=
XM_011540044.1:c.2070_2071delinsCT	XP_011538346.1:p.Thr690=
XM_011540045.1:c.2205_2206delinsCT	XP_011538347.1:p.Thr735=
XM_011540046.1:c.1665_1666delinsCT	XP_011538348.1:p.Thr555=
XM_011540047.1:c.1023_1024delinsCT	XP_011538349.1:p.Thr341=
XM_011540048.1:c.2205_2206delinsCT	XP_011538350.1:p.Thr735=
XM_011540049.1:c.2205_2206delinsCT	XP_011538351.1:p.Thr735=
XM_011540050.1:c.2205_2206delinsCT	XP_011538352.1:p.Thr735=
XM_011540051.1:c.2205_2206delinsCT	XP_011538353.1:p.Thr735=
XM_011540053.1:c.2205_2206delinsCT	XP_011538355.1:p.Thr735=
XM_011540054.1:c.2145_2146delinsCT	XP_011538356.1:p.Thr715=
XR_945796.1:n.2448_2449delinsCT
NM_001171930.2:c.2010_2011delinsCT	NP_001165401.1:p.Thr670=
NM_001171931.2:c.2010_2011delinsCT	NP_001165402.1:p.Thr670=
NM_022124.6:c.2010_2011delinsCT MANE Select	NP_071407.4:p.Thr670=