Canonical Allele Identifier: CA2788462039

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71687747_71687748del , CM000672.2:g.71687747_71687748del	GRCh38
NC_000010.10:g.73447504_73447505del , CM000672.1:g.73447504_73447505del	GRCh37
NC_000010.9:g.73117510_73117511del	NCBI36
NG_008835.1:g.295801_295802del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.2059+28_2059+29del MANE Select	ENSP00000224721.9:n.2059+28_2059+29del
ENST00000398809.9:c.2059+28_2059+29del	ENSP00000381789.5:n.2059+28_2059+29del
ENST00000442677.4:c.2059+28_2059+29del	ENSP00000388894.3:n.2059+28_2059+29del
ENST00000466757.8:c.1490+28_1490+29del
ENST00000224721.10:c.2074+28_2074+29del	ENSP00000224721.8:n.2074+28_2074+29del
ENST00000299366.11:c.2059+28_2059+29del	ENSP00000299366.8:n.2059+28_2059+29del
ENST00000398809.8:c.2059+28_2059+29del	ENSP00000381789.5:n.2059+28_2059+29del
ENST00000442677.3:c.834+28_834+29del
ENST00000466757.7:c.1490+28_1490+29del
ENST00000616684.4:c.2059+28_2059+29del	ENSP00000482036.2:n.2059+28_2059+29del
ENST00000622827.4:c.2059+28_2059+29del	ENSP00000483211.1:n.2059+28_2059+29del
NM_001171930.1:c.2059+28_2059+29del	NP_001165401.1:n.2059+28_2059+29del
NM_001171931.1:c.2059+28_2059+29del	NP_001165402.1:n.2059+28_2059+29del
NM_022124.5:c.2059+28_2059+29del	NP_071407.4:n.2059+28_2059+29del
XM_006717940.2:c.2254+28_2254+29del	XP_006718003.1:n.2254+28_2254+29del
XM_006717942.2:c.2188+28_2188+29del	XP_006718005.1:n.2188+28_2188+29del
XM_011540039.1:c.2254+28_2254+29del	XP_011538341.1:n.2254+28_2254+29del
XM_011540040.1:c.2248+28_2248+29del	XP_011538342.1:n.2248+28_2248+29del
XM_011540041.1:c.2194+28_2194+29del	XP_011538343.1:n.2194+28_2194+29del
XM_011540042.1:c.2254+28_2254+29del	XP_011538344.1:n.2254+28_2254+29del
XM_011540043.1:c.2254+28_2254+29del	XP_011538345.1:n.2254+28_2254+29del
XM_011540044.1:c.2119+28_2119+29del	XP_011538346.1:n.2119+28_2119+29del
XM_011540045.1:c.2254+28_2254+29del	XP_011538347.1:n.2254+28_2254+29del
XM_011540046.1:c.1714+28_1714+29del	XP_011538348.1:n.1714+28_1714+29del
XM_011540047.1:c.1072+28_1072+29del	XP_011538349.1:n.1072+28_1072+29del
XM_011540048.1:c.2254+28_2254+29del	XP_011538350.1:n.2254+28_2254+29del
XM_011540049.1:c.2254+28_2254+29del	XP_011538351.1:n.2254+28_2254+29del
XM_011540050.1:c.2254+28_2254+29del	XP_011538352.1:n.2254+28_2254+29del
XM_011540051.1:c.2254+28_2254+29del	XP_011538353.1:n.2254+28_2254+29del
XM_011540053.1:c.2254+28_2254+29del	XP_011538355.1:n.2254+28_2254+29del
XM_011540054.1:c.2194+28_2194+29del	XP_011538356.1:n.2194+28_2194+29del
XR_945796.1:n.2497+28_2497+29del
NM_001171930.2:c.2059+28_2059+29del	NP_001165401.1:n.2059+28_2059+29del
NM_001171931.2:c.2059+28_2059+29del	NP_001165402.1:n.2059+28_2059+29del
NM_022124.6:c.2059+28_2059+29del MANE Select	NP_071407.4:n.2059+28_2059+29del