Canonical Allele Identifier: CA470068782

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71738644G>A , CM000672.2:g.71738644G>A	GRCh38
NC_000010.10:g.73498401G>A , CM000672.1:g.73498401G>A	GRCh37
NC_000010.9:g.73168407G>A	NCBI36
NG_008835.1:g.346698G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.4356G>A MANE Select	NP_071407.4:p.Gly1452=
ENST00000224721.12:c.4356G>A MANE Select	ENSP00000224721.9:p.Gly1452=
NM_022124.5:c.4356G>A	NP_071407.4:p.Gly1452=
ENST00000224721.10:c.4371G>A	ENSP00000224721.8:p.Gly1457=
ENST00000398792.3:n.1045G>A
ENST00000622827.4:c.4356G>A	ENSP00000483211.1:p.Gly1452=
XM_006717940.2:c.4551G>A	XP_006718003.1:p.Gly1517=
XM_006717942.2:c.4485G>A	XP_006718005.1:p.Gly1495=
XM_011540039.1:c.4548G>A	XP_011538341.1:p.Gly1516=
XM_011540040.1:c.4545G>A	XP_011538342.1:p.Gly1515=
XM_011540041.1:c.4491G>A	XP_011538343.1:p.Gly1497=
XM_011540042.1:c.4551G>A	XP_011538344.1:p.Gly1517=
XM_011540043.1:c.4551G>A	XP_011538345.1:p.Gly1517=
XM_011540044.1:c.4416G>A	XP_011538346.1:p.Gly1472=
XM_011540045.1:c.4551G>A	XP_011538347.1:p.Gly1517=
XM_011540046.1:c.4011G>A	XP_011538348.1:p.Gly1337=
XM_011540047.1:c.3369G>A	XP_011538349.1:p.Gly1123=
XM_011540048.1:c.4551G>A	XP_011538350.1:p.Gly1517=
XM_011540049.1:c.4551G>A	XP_011538351.1:p.Gly1517=
XM_011540050.1:c.4551G>A	XP_011538352.1:p.Gly1517=
XM_011540051.1:c.4551G>A	XP_011538353.1:p.Gly1517=
XM_011540052.1:c.879G>A	XP_011538354.1:p.Gly293=
XM_011540053.1:c.4551G>A	XP_011538355.1:p.Gly1517=
XR_945796.1:n.4794G>A