Canonical Allele Identifier: CA1918853836

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740853G= , CM000672.2:g.71740853G=	GRCh38
NC_000010.10:g.73500610G= , CM000672.1:g.73500610G=	GRCh37
NC_000010.9:g.73170616G=	NCBI36
NG_008835.1:g.348907G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.4520G= MANE Select	ENSP00000224721.9:p.Arg1507=
ENST00000224721.10:c.4535G=	ENSP00000224721.8:p.Arg1512=
ENST00000398792.3:n.1209G=
ENST00000622827.4:c.4520G=	ENSP00000483211.1:p.Arg1507=
NM_022124.5:c.4520G=	NP_071407.4:p.Arg1507=
XM_006717940.2:c.4715G=	XP_006718003.1:p.Arg1572=
XM_006717942.2:c.4649G=	XP_006718005.1:p.Arg1550=
XM_011540039.1:c.4712G=	XP_011538341.1:p.Arg1571=
XM_011540040.1:c.4709G=	XP_011538342.1:p.Arg1570=
XM_011540041.1:c.4655G=	XP_011538343.1:p.Arg1552=
XM_011540042.1:c.4715G=	XP_011538344.1:p.Arg1572=
XM_011540043.1:c.4715G=	XP_011538345.1:p.Arg1572=
XM_011540044.1:c.4580G=	XP_011538346.1:p.Arg1527=
XM_011540045.1:c.4715G=	XP_011538347.1:p.Arg1572=
XM_011540046.1:c.4175G=	XP_011538348.1:p.Arg1392=
XM_011540047.1:c.3533G=	XP_011538349.1:p.Arg1178=
XM_011540048.1:c.4715G=	XP_011538350.1:p.Arg1572=
XM_011540049.1:c.4715G=	XP_011538351.1:p.Arg1572=
XM_011540050.1:c.4715G=	XP_011538352.1:p.Arg1572=
XM_011540051.1:c.4715G=	XP_011538353.1:p.Arg1572=
XM_011540052.1:c.1043G=	XP_011538354.1:p.Arg348=
XM_011540053.1:c.4715G=	XP_011538355.1:p.Arg1572=
XR_945796.1:n.4958G=
NM_022124.6:c.4520G= MANE Select	NP_071407.4:p.Arg1507=