Canonical Allele Identifier: CA137355

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71707035G>C , CM000672.2:g.71707035G>C	GRCh38
NC_000010.10:g.73466792G>C , CM000672.1:g.73466792G>C	GRCh37
NC_000010.9:g.73136798G>C	NCBI36
NG_008835.1:g.315089G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.3092G>C MANE Select	ENSP00000224721.9:p.Ser1031Thr
ENST00000398809.9:c.3092G>C	ENSP00000381789.5:p.Ser1031Thr
ENST00000442677.4:c.3092G>C	ENSP00000388894.3:p.Ser1031Thr
ENST00000466757.8:c.2523G>C
ENST00000224721.10:c.3107G>C	ENSP00000224721.8:p.Ser1036Thr
ENST00000299366.11:c.3092G>C	ENSP00000299366.8:p.Ser1031Thr
ENST00000398809.8:c.3092G>C	ENSP00000381789.5:p.Ser1031Thr
ENST00000442677.3:c.1867G>C
ENST00000466757.7:c.2523G>C
ENST00000616684.4:c.3092G>C	ENSP00000482036.2:p.Ser1031Thr
ENST00000622827.4:c.3092G>C	ENSP00000483211.1:p.Ser1031Thr
NM_001171930.1:c.3092G>C	NP_001165401.1:p.Ser1031Thr
NM_001171931.1:c.3092G>C	NP_001165402.1:p.Ser1031Thr
NM_022124.5:c.3092G>C	NP_071407.4:p.Ser1031Thr
XM_006717940.2:c.3287G>C	XP_006718003.1:p.Ser1096Thr
XM_006717942.2:c.3221G>C	XP_006718005.1:p.Ser1074Thr
XM_011540039.1:c.3287G>C	XP_011538341.1:p.Ser1096Thr
XM_011540040.1:c.3281G>C	XP_011538342.1:p.Ser1094Thr
XM_011540041.1:c.3227G>C	XP_011538343.1:p.Ser1076Thr
XM_011540042.1:c.3287G>C	XP_011538344.1:p.Ser1096Thr
XM_011540043.1:c.3287G>C	XP_011538345.1:p.Ser1096Thr
XM_011540044.1:c.3152G>C	XP_011538346.1:p.Ser1051Thr
XM_011540045.1:c.3287G>C	XP_011538347.1:p.Ser1096Thr
XM_011540046.1:c.2747G>C	XP_011538348.1:p.Ser916Thr
XM_011540047.1:c.2105G>C	XP_011538349.1:p.Ser702Thr
XM_011540048.1:c.3287G>C	XP_011538350.1:p.Ser1096Thr
XM_011540049.1:c.3287G>C	XP_011538351.1:p.Ser1096Thr
XM_011540050.1:c.3287G>C	XP_011538352.1:p.Ser1096Thr
XM_011540051.1:c.3287G>C	XP_011538353.1:p.Ser1096Thr
XM_011540053.1:c.3287G>C	XP_011538355.1:p.Ser1096Thr
XM_011540054.1:c.3227G>C	XP_011538356.1:p.Ser1076Thr
XR_945796.1:n.3530G>C
XR_946052.1:n.82+1971C>G
NM_001171930.2:c.3092G>C	NP_001165401.1:p.Ser1031Thr
NM_001171931.2:c.3092G>C	NP_001165402.1:p.Ser1031Thr
NM_022124.6:c.3092G>C MANE Select	NP_071407.4:p.Ser1031Thr