Canonical Allele Identifier: CA1918809228

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71645825_71645826delinsAC , CM000672.2:g.71645825_71645826delinsAC	GRCh38
NC_000010.10:g.73405582_73405583delinsAC , CM000672.1:g.73405582_73405583delinsAC	GRCh37
NC_000010.9:g.73075588_73075589delinsAC	NCBI36
NG_008835.1:g.253879_253880delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.1141-6_1141-5delinsAC MANE Select	ENSP00000224721.9:n.1141-6_1141-5delinsAC
ENST00000398809.9:c.1141-6_1141-5delinsAC	ENSP00000381789.5:n.1141-6_1141-5delinsAC
ENST00000442677.4:c.1141-6_1141-5delinsAC	ENSP00000388894.3:n.1141-6_1141-5delinsAC
ENST00000466757.8:c.572-6_572-5delinsAC
ENST00000643732.1:n.977-6_977-5delinsAC
ENST00000646131.1:c.805-6_805-5delinsAC	ENSP00000495098.1:n.805-6_805-5delinsAC
ENST00000224721.10:c.1156-6_1156-5delinsAC	ENSP00000224721.8:n.1156-6_1156-5delinsAC
ENST00000299366.11:c.1141-6_1141-5delinsAC	ENSP00000299366.8:n.1141-6_1141-5delinsAC
ENST00000398809.8:c.1141-6_1141-5delinsAC	ENSP00000381789.5:n.1141-6_1141-5delinsAC
ENST00000398842.7:c.886-6_886-5delinsAC	ENSP00000381822.4:n.886-6_886-5delinsAC
ENST00000461841.7:c.1141-6_1141-5delinsAC	ENSP00000473454.2:n.1141-6_1141-5delinsAC
ENST00000466757.7:c.572-6_572-5delinsAC
ENST00000470494.5:c.110-6_110-5delinsAC
ENST00000616684.4:c.1141-6_1141-5delinsAC	ENSP00000482036.2:n.1141-6_1141-5delinsAC
ENST00000622827.4:c.1135_1136delinsAC	ENSP00000483211.1:p.Thr379=
NM_001171930.1:c.1141-6_1141-5delinsAC	NP_001165401.1:n.1141-6_1141-5delinsAC
NM_001171931.1:c.1141-6_1141-5delinsAC	NP_001165402.1:n.1141-6_1141-5delinsAC
NM_022124.5:c.1141-6_1141-5delinsAC	NP_071407.4:n.1141-6_1141-5delinsAC
NM_052836.3:c.1141-6_1141-5delinsAC	NP_443068.1:n.1141-6_1141-5delinsAC
XM_006717940.2:c.1336-6_1336-5delinsAC	XP_006718003.1:n.1336-6_1336-5delinsAC
XM_006717942.2:c.1270-6_1270-5delinsAC	XP_006718005.1:n.1270-6_1270-5delinsAC
XM_011540039.1:c.1336-6_1336-5delinsAC	XP_011538341.1:n.1336-6_1336-5delinsAC
XM_011540040.1:c.1330-6_1330-5delinsAC	XP_011538342.1:n.1330-6_1330-5delinsAC
XM_011540041.1:c.1276-6_1276-5delinsAC	XP_011538343.1:n.1276-6_1276-5delinsAC
XM_011540042.1:c.1336-6_1336-5delinsAC	XP_011538344.1:n.1336-6_1336-5delinsAC
XM_011540043.1:c.1336-6_1336-5delinsAC	XP_011538345.1:n.1336-6_1336-5delinsAC
XM_011540044.1:c.1201-6_1201-5delinsAC	XP_011538346.1:n.1201-6_1201-5delinsAC
XM_011540045.1:c.1336-6_1336-5delinsAC	XP_011538347.1:n.1336-6_1336-5delinsAC
XM_011540046.1:c.796-6_796-5delinsAC	XP_011538348.1:n.796-6_796-5delinsAC
XM_011540047.1:c.154-6_154-5delinsAC	XP_011538349.1:n.154-6_154-5delinsAC
XM_011540048.1:c.1336-6_1336-5delinsAC	XP_011538350.1:n.1336-6_1336-5delinsAC
XM_011540049.1:c.1336-6_1336-5delinsAC	XP_011538351.1:n.1336-6_1336-5delinsAC
XM_011540050.1:c.1336-6_1336-5delinsAC	XP_011538352.1:n.1336-6_1336-5delinsAC
XM_011540051.1:c.1336-6_1336-5delinsAC	XP_011538353.1:n.1336-6_1336-5delinsAC
XM_011540053.1:c.1336-6_1336-5delinsAC	XP_011538355.1:n.1336-6_1336-5delinsAC
XM_011540054.1:c.1276-6_1276-5delinsAC	XP_011538356.1:n.1276-6_1276-5delinsAC
XR_945796.1:n.1579-6_1579-5delinsAC
NM_001171930.2:c.1141-6_1141-5delinsAC	NP_001165401.1:n.1141-6_1141-5delinsAC
NM_001171931.2:c.1141-6_1141-5delinsAC	NP_001165402.1:n.1141-6_1141-5delinsAC
NM_022124.6:c.1141-6_1141-5delinsAC MANE Select	NP_071407.4:n.1141-6_1141-5delinsAC
NM_052836.4:c.1141-6_1141-5delinsAC	NP_443068.1:n.1141-6_1141-5delinsAC