Canonical Allele Identifier: CA1918874173

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793248G= , CM000672.2:g.71793248G=	GRCh38
NC_000010.10:g.73553005G= , CM000672.1:g.73553005G=	GRCh37
NC_000010.9:g.73223011G=	NCBI36
NG_008835.1:g.401302G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6320G= MANE Select	ENSP00000224721.9:p.Arg2107=
ENST00000224721.10:c.6335G=	ENSP00000224721.8:p.Arg2112=
ENST00000622827.4:c.6320G=	ENSP00000483211.1:p.Arg2107=
NM_022124.5:c.6320G=	NP_071407.4:p.Arg2107=
XM_006717940.2:c.6515G=	XP_006718003.1:p.Arg2172=
XM_006717942.2:c.6449G=	XP_006718005.1:p.Arg2150=
XM_011540039.1:c.6512G=	XP_011538341.1:p.Arg2171=
XM_011540040.1:c.6509G=	XP_011538342.1:p.Arg2170=
XM_011540041.1:c.6455G=	XP_011538343.1:p.Arg2152=
XM_011540042.1:c.6515G=	XP_011538344.1:p.Arg2172=
XM_011540043.1:c.6515G=	XP_011538345.1:p.Arg2172=
XM_011540044.1:c.6380G=	XP_011538346.1:p.Arg2127=
XM_011540045.1:c.6515G=	XP_011538347.1:p.Arg2172=
XM_011540046.1:c.5975G=	XP_011538348.1:p.Arg1992=
XM_011540047.1:c.5333G=	XP_011538349.1:p.Arg1778=
XM_011540048.1:c.6515G=	XP_011538350.1:p.Arg2172=
XM_011540049.1:c.6515G=	XP_011538351.1:p.Arg2172=
XM_011540050.1:c.6515G=	XP_011538352.1:p.Arg2172=
XM_011540051.1:c.6515G=	XP_011538353.1:p.Arg2172=
XM_011540052.1:c.2843G=	XP_011538354.1:p.Arg948=
XR_945796.1:n.6758G=
NM_022124.6:c.6320G= MANE Select	NP_071407.4:p.Arg2107=