Canonical Allele Identifier: CA1918861803

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784805C= , CM000672.2:g.71784805C=	GRCh38
NC_000010.10:g.73544562C= , CM000672.1:g.73544562C=	GRCh37
NC_000010.9:g.73214568C=	NCBI36
NG_008835.1:g.392859C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5503-86C= MANE Select	ENSP00000224721.9:n.5503-86C=
ENST00000224721.10:c.5518-86C=	ENSP00000224721.8:n.5518-86C=
ENST00000622827.4:c.5503-86C=	ENSP00000483211.1:n.5503-86C=
NM_022124.5:c.5503-86C=	NP_071407.4:n.5503-86C=
XM_006717940.2:c.5698-86C=	XP_006718003.1:n.5698-86C=
XM_006717942.2:c.5632-86C=	XP_006718005.1:n.5632-86C=
XM_011540039.1:c.5695-86C=	XP_011538341.1:n.5695-86C=
XM_011540040.1:c.5692-86C=	XP_011538342.1:n.5692-86C=
XM_011540041.1:c.5638-86C=	XP_011538343.1:n.5638-86C=
XM_011540042.1:c.5698-86C=	XP_011538344.1:n.5698-86C=
XM_011540043.1:c.5698-86C=	XP_011538345.1:n.5698-86C=
XM_011540044.1:c.5563-86C=	XP_011538346.1:n.5563-86C=
XM_011540045.1:c.5698-86C=	XP_011538347.1:n.5698-86C=
XM_011540046.1:c.5158-86C=	XP_011538348.1:n.5158-86C=
XM_011540047.1:c.4516-86C=	XP_011538349.1:n.4516-86C=
XM_011540048.1:c.5698-86C=	XP_011538350.1:n.5698-86C=
XM_011540049.1:c.5698-86C=	XP_011538351.1:n.5698-86C=
XM_011540050.1:c.5698-86C=	XP_011538352.1:n.5698-86C=
XM_011540051.1:c.5698-86C=	XP_011538353.1:n.5698-86C=
XM_011540052.1:c.2026-86C=	XP_011538354.1:n.2026-86C=
XM_011540053.1:c.5698-86C=	XP_011538355.1:n.5698-86C=
XR_945796.1:n.5941-86C=
NM_022124.6:c.5503-86C= MANE Select	NP_071407.4:n.5503-86C=