Canonical Allele Identifier: CA2609570226

Gene: CDH23

Linked Data

• gnomAD v4: 10-71709260-ACACAGGGTGCCTCCCAGGAGCTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71709261_71709283del , CM000672.2:g.71709261_71709283del	GRCh38
NC_000010.10:g.73469018_73469040del , CM000672.1:g.73469018_73469040del	GRCh37
NC_000010.9:g.73139024_73139046del	NCBI36
NG_008835.1:g.317315_317337del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.3220+50_3220+72del MANE Select	ENSP00000224721.9:n.3220+50_3220+72del
ENST00000398809.9:c.3220+50_3220+72del	ENSP00000381789.5:n.3220+50_3220+72del
ENST00000442677.4:c.3220+50_3220+72del	ENSP00000388894.3:n.3220+50_3220+72del
ENST00000466757.8:c.2651+50_2651+72del
ENST00000224721.10:c.3235+50_3235+72del	ENSP00000224721.8:n.3235+50_3235+72del
ENST00000398809.8:c.3220+50_3220+72del	ENSP00000381789.5:n.3220+50_3220+72del
ENST00000442677.3:c.1995+50_1995+72del
ENST00000466757.7:c.2651+50_2651+72del
ENST00000616684.4:c.3220+50_3220+72del	ENSP00000482036.2:n.3220+50_3220+72del
ENST00000622827.4:c.3220+50_3220+72del	ENSP00000483211.1:n.3220+50_3220+72del
NM_001171930.1:c.3220+50_3220+72del	NP_001165401.1:n.3220+50_3220+72del
NM_022124.5:c.3220+50_3220+72del	NP_071407.4:n.3220+50_3220+72del
XM_006717940.2:c.3415+50_3415+72del	XP_006718003.1:n.3415+50_3415+72del
XM_006717942.2:c.3349+50_3349+72del	XP_006718005.1:n.3349+50_3349+72del
XM_011540039.1:c.3415+50_3415+72del	XP_011538341.1:n.3415+50_3415+72del
XM_011540040.1:c.3409+50_3409+72del	XP_011538342.1:n.3409+50_3409+72del
XM_011540041.1:c.3355+50_3355+72del	XP_011538343.1:n.3355+50_3355+72del
XM_011540042.1:c.3415+50_3415+72del	XP_011538344.1:n.3415+50_3415+72del
XM_011540043.1:c.3415+50_3415+72del	XP_011538345.1:n.3415+50_3415+72del
XM_011540044.1:c.3280+50_3280+72del	XP_011538346.1:n.3280+50_3280+72del
XM_011540045.1:c.3415+50_3415+72del	XP_011538347.1:n.3415+50_3415+72del
XM_011540046.1:c.2875+50_2875+72del	XP_011538348.1:n.2875+50_2875+72del
XM_011540047.1:c.2233+50_2233+72del	XP_011538349.1:n.2233+50_2233+72del
XM_011540048.1:c.3415+50_3415+72del	XP_011538350.1:n.3415+50_3415+72del
XM_011540049.1:c.3415+50_3415+72del	XP_011538351.1:n.3415+50_3415+72del
XM_011540050.1:c.3415+50_3415+72del	XP_011538352.1:n.3415+50_3415+72del
XM_011540051.1:c.3415+50_3415+72del	XP_011538353.1:n.3415+50_3415+72del
XM_011540053.1:c.3415+50_3415+72del	XP_011538355.1:n.3415+50_3415+72del
XR_945796.1:n.3658+50_3658+72del
NM_001171930.2:c.3220+50_3220+72del	NP_001165401.1:n.3220+50_3220+72del
NM_022124.6:c.3220+50_3220+72del MANE Select	NP_071407.4:n.3220+50_3220+72del