Canonical Allele Identifier: CA2788479402

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71709310_71709327del , CM000672.2:g.71709310_71709327del	GRCh38
NC_000010.10:g.73469067_73469084del , CM000672.1:g.73469067_73469084del	GRCh37
NC_000010.9:g.73139073_73139090del	NCBI36
NG_008835.1:g.317364_317381del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.3220+99_3220+116del MANE Select	ENSP00000224721.9:n.3220+99_3220+116del
ENST00000398809.9:c.3220+99_3220+116del	ENSP00000381789.5:n.3220+99_3220+116del
ENST00000442677.4:c.3220+99_3220+116del	ENSP00000388894.3:n.3220+99_3220+116del
ENST00000466757.8:c.2651+99_2651+116del
ENST00000224721.10:c.3235+99_3235+116del	ENSP00000224721.8:n.3235+99_3235+116del
ENST00000398809.8:c.3220+99_3220+116del	ENSP00000381789.5:n.3220+99_3220+116del
ENST00000442677.3:c.1995+99_1995+116del
ENST00000466757.7:c.2651+99_2651+116del
ENST00000616684.4:c.3220+99_3220+116del	ENSP00000482036.2:n.3220+99_3220+116del
ENST00000622827.4:c.3220+99_3220+116del	ENSP00000483211.1:n.3220+99_3220+116del
NM_001171930.1:c.3220+99_3220+116del	NP_001165401.1:n.3220+99_3220+116del
NM_022124.5:c.3220+99_3220+116del	NP_071407.4:n.3220+99_3220+116del
XM_006717940.2:c.3415+99_3415+116del	XP_006718003.1:n.3415+99_3415+116del
XM_006717942.2:c.3349+99_3349+116del	XP_006718005.1:n.3349+99_3349+116del
XM_011540039.1:c.3415+99_3415+116del	XP_011538341.1:n.3415+99_3415+116del
XM_011540040.1:c.3409+99_3409+116del	XP_011538342.1:n.3409+99_3409+116del
XM_011540041.1:c.3355+99_3355+116del	XP_011538343.1:n.3355+99_3355+116del
XM_011540042.1:c.3415+99_3415+116del	XP_011538344.1:n.3415+99_3415+116del
XM_011540043.1:c.3415+99_3415+116del	XP_011538345.1:n.3415+99_3415+116del
XM_011540044.1:c.3280+99_3280+116del	XP_011538346.1:n.3280+99_3280+116del
XM_011540045.1:c.3415+99_3415+116del	XP_011538347.1:n.3415+99_3415+116del
XM_011540046.1:c.2875+99_2875+116del	XP_011538348.1:n.2875+99_2875+116del
XM_011540047.1:c.2233+99_2233+116del	XP_011538349.1:n.2233+99_2233+116del
XM_011540048.1:c.3415+99_3415+116del	XP_011538350.1:n.3415+99_3415+116del
XM_011540049.1:c.3415+99_3415+116del	XP_011538351.1:n.3415+99_3415+116del
XM_011540050.1:c.3415+99_3415+116del	XP_011538352.1:n.3415+99_3415+116del
XM_011540051.1:c.3415+99_3415+116del	XP_011538353.1:n.3415+99_3415+116del
XM_011540053.1:c.3415+99_3415+116del	XP_011538355.1:n.3415+99_3415+116del
XR_945796.1:n.3658+99_3658+116del
NM_001171930.2:c.3220+99_3220+116del	NP_001165401.1:n.3220+99_3220+116del
NM_022124.6:c.3220+99_3220+116del MANE Select	NP_071407.4:n.3220+99_3220+116del