Canonical Allele Identifier: CA1918875380

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71779316G= , CM000672.2:g.71779316G=	GRCh38
NC_000010.10:g.73539073G= , CM000672.1:g.73539073G=	GRCh37
NC_000010.9:g.73209079G=	NCBI36
NG_008835.1:g.387370G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5237G= MANE Select	ENSP00000224721.9:p.Arg1746=
ENST00000224721.10:c.5252G=	ENSP00000224721.8:p.Arg1751=
ENST00000622827.4:c.5237G=	ENSP00000483211.1:p.Arg1746=
NM_022124.5:c.5237G=	NP_071407.4:p.Arg1746=
XM_006717940.2:c.5432G=	XP_006718003.1:p.Arg1811=
XM_006717942.2:c.5366G=	XP_006718005.1:p.Arg1789=
XM_011540039.1:c.5429G=	XP_011538341.1:p.Arg1810=
XM_011540040.1:c.5426G=	XP_011538342.1:p.Arg1809=
XM_011540041.1:c.5372G=	XP_011538343.1:p.Arg1791=
XM_011540042.1:c.5432G=	XP_011538344.1:p.Arg1811=
XM_011540043.1:c.5432G=	XP_011538345.1:p.Arg1811=
XM_011540044.1:c.5297G=	XP_011538346.1:p.Arg1766=
XM_011540045.1:c.5432G=	XP_011538347.1:p.Arg1811=
XM_011540046.1:c.4892G=	XP_011538348.1:p.Arg1631=
XM_011540047.1:c.4250G=	XP_011538349.1:p.Arg1417=
XM_011540048.1:c.5432G=	XP_011538350.1:p.Arg1811=
XM_011540049.1:c.5432G=	XP_011538351.1:p.Arg1811=
XM_011540050.1:c.5432G=	XP_011538352.1:p.Arg1811=
XM_011540051.1:c.5432G=	XP_011538353.1:p.Arg1811=
XM_011540052.1:c.1760G=	XP_011538354.1:p.Arg587=
XM_011540053.1:c.5432G=	XP_011538355.1:p.Arg1811=
XR_945796.1:n.5675G=
NM_022124.6:c.5237G= MANE Select	NP_071407.4:p.Arg1746=