Canonical Allele Identifier: CA1918853847

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740875G= , CM000672.2:g.71740875G=	GRCh38
NC_000010.10:g.73500632G= , CM000672.1:g.73500632G=	GRCh37
NC_000010.9:g.73170638G=	NCBI36
NG_008835.1:g.348929G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4542G= MANE Select	ENSP00000224721.9:p.Gln1514=
ENST00000224721.10:c.4557G=	ENSP00000224721.8:p.Gln1519=
ENST00000398792.3:n.1231G=
ENST00000622827.4:c.4542G=	ENSP00000483211.1:p.Gln1514=
NM_022124.5:c.4542G=	NP_071407.4:p.Gln1514=
XM_006717940.2:c.4737G=	XP_006718003.1:p.Gln1579=
XM_006717942.2:c.4671G=	XP_006718005.1:p.Gln1557=
XM_011540039.1:c.4734G=	XP_011538341.1:p.Gln1578=
XM_011540040.1:c.4731G=	XP_011538342.1:p.Gln1577=
XM_011540041.1:c.4677G=	XP_011538343.1:p.Gln1559=
XM_011540042.1:c.4737G=	XP_011538344.1:p.Gln1579=
XM_011540043.1:c.4737G=	XP_011538345.1:p.Gln1579=
XM_011540044.1:c.4602G=	XP_011538346.1:p.Gln1534=
XM_011540045.1:c.4737G=	XP_011538347.1:p.Gln1579=
XM_011540046.1:c.4197G=	XP_011538348.1:p.Gln1399=
XM_011540047.1:c.3555G=	XP_011538349.1:p.Gln1185=
XM_011540048.1:c.4737G=	XP_011538350.1:p.Gln1579=
XM_011540049.1:c.4737G=	XP_011538351.1:p.Gln1579=
XM_011540050.1:c.4737G=	XP_011538352.1:p.Gln1579=
XM_011540051.1:c.4737G=	XP_011538353.1:p.Gln1579=
XM_011540052.1:c.1065G=	XP_011538354.1:p.Gln355=
XM_011540053.1:c.4737G=	XP_011538355.1:p.Gln1579=
XR_945796.1:n.4980G=
NM_022124.6:c.4542G= MANE Select	NP_071407.4:p.Gln1514=