Canonical Allele Identifier: CA2788474766

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71571015_71571016insAGA , CM000672.2:g.71571015_71571016insAGA	GRCh38
NC_000010.10:g.73330772_73330773insAGA , CM000672.1:g.73330772_73330773insAGA	GRCh37
NC_000010.9:g.73000778_73000779insAGA	NCBI36
NG_008835.1:g.179069_179070insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.753+97_753+98insAGA MANE Select	ENSP00000224721.9:n.753+97_753+98insAGA
ENST00000398809.9:c.753+97_753+98insAGA	ENSP00000381789.5:n.753+97_753+98insAGA
ENST00000442677.4:c.753+97_753+98insAGA	ENSP00000388894.3:n.753+97_753+98insAGA
ENST00000466757.8:c.124+97_124+98insAGA
ENST00000643732.1:n.529+97_529+98insAGA
ENST00000646131.1:c.417+97_417+98insAGA	ENSP00000495098.1:n.417+97_417+98insAGA
ENST00000224721.10:c.768+97_768+98insAGA	ENSP00000224721.8:n.768+97_768+98insAGA
ENST00000299366.11:c.753+97_753+98insAGA	ENSP00000299366.8:n.753+97_753+98insAGA
ENST00000398809.8:c.753+97_753+98insAGA	ENSP00000381789.5:n.753+97_753+98insAGA
ENST00000398842.7:c.504+97_504+98insAGA	ENSP00000381822.4:n.504+97_504+98insAGA
ENST00000461841.7:c.753+97_753+98insAGA	ENSP00000473454.2:n.753+97_753+98insAGA
ENST00000466757.7:c.124+97_124+98insAGA
ENST00000616684.4:c.753+97_753+98insAGA	ENSP00000482036.2:n.753+97_753+98insAGA
ENST00000622827.4:c.753+97_753+98insAGA	ENSP00000483211.1:n.753+97_753+98insAGA
NM_001171930.1:c.753+97_753+98insAGA	NP_001165401.1:n.753+97_753+98insAGA
NM_001171931.1:c.753+97_753+98insAGA	NP_001165402.1:n.753+97_753+98insAGA
NM_001171932.1:c.753+97_753+98insAGA	NP_001165403.1:n.753+97_753+98insAGA
NM_022124.5:c.753+97_753+98insAGA	NP_071407.4:n.753+97_753+98insAGA
NM_052836.3:c.753+97_753+98insAGA	NP_443068.1:n.753+97_753+98insAGA
XM_006717940.2:c.888+97_888+98insAGA	XP_006718003.1:n.888+97_888+98insAGA
XM_006717942.2:c.888+97_888+98insAGA	XP_006718005.1:n.888+97_888+98insAGA
XM_011540039.1:c.888+97_888+98insAGA	XP_011538341.1:n.888+97_888+98insAGA
XM_011540040.1:c.888+97_888+98insAGA	XP_011538342.1:n.888+97_888+98insAGA
XM_011540041.1:c.888+97_888+98insAGA	XP_011538343.1:n.888+97_888+98insAGA
XM_011540042.1:c.888+97_888+98insAGA	XP_011538344.1:n.888+97_888+98insAGA
XM_011540043.1:c.888+97_888+98insAGA	XP_011538345.1:n.888+97_888+98insAGA
XM_011540044.1:c.753+97_753+98insAGA	XP_011538346.1:n.753+97_753+98insAGA
XM_011540045.1:c.888+97_888+98insAGA	XP_011538347.1:n.888+97_888+98insAGA
XM_011540046.1:c.348+97_348+98insAGA	XP_011538348.1:n.348+97_348+98insAGA
XM_011540048.1:c.888+97_888+98insAGA	XP_011538350.1:n.888+97_888+98insAGA
XM_011540049.1:c.888+97_888+98insAGA	XP_011538351.1:n.888+97_888+98insAGA
XM_011540050.1:c.888+97_888+98insAGA	XP_011538352.1:n.888+97_888+98insAGA
XM_011540051.1:c.888+97_888+98insAGA	XP_011538353.1:n.888+97_888+98insAGA
XM_011540053.1:c.888+97_888+98insAGA	XP_011538355.1:n.888+97_888+98insAGA
XM_011540054.1:c.888+97_888+98insAGA	XP_011538356.1:n.888+97_888+98insAGA
XR_246128.2:n.162-5882_162-5881insTCT
XR_945796.1:n.1131+97_1131+98insAGA
NM_001171930.2:c.753+97_753+98insAGA	NP_001165401.1:n.753+97_753+98insAGA
NM_001171931.2:c.753+97_753+98insAGA	NP_001165402.1:n.753+97_753+98insAGA
NM_022124.6:c.753+97_753+98insAGA MANE Select	NP_071407.4:n.753+97_753+98insAGA
NM_052836.4:c.753+97_753+98insAGA	NP_443068.1:n.753+97_753+98insAGA
NM_001171932.2:c.753+97_753+98insAGA	NP_001165403.1:n.753+97_753+98insAGA