Canonical Allele Identifier: CA1918852716

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71738597C= , CM000672.2:g.71738597C=	GRCh38
NC_000010.10:g.73498354C= , CM000672.1:g.73498354C=	GRCh37
NC_000010.9:g.73168360C=	NCBI36
NG_008835.1:g.346651C=

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.4309C= MANE Select	NP_071407.4:p.Arg1437=
ENST00000224721.12:c.4309C= MANE Select	ENSP00000224721.9:p.Arg1437=
NM_022124.5:c.4309C=	NP_071407.4:p.Arg1437=
ENST00000224721.10:c.4324C=	ENSP00000224721.8:p.Arg1442=
ENST00000398792.3:n.998C=
ENST00000622827.4:c.4309C=	ENSP00000483211.1:p.Arg1437=
XM_006717940.2:c.4504C=	XP_006718003.1:p.Arg1502=
XM_006717942.2:c.4438C=	XP_006718005.1:p.Arg1480=
XM_011540039.1:c.4501C=	XP_011538341.1:p.Arg1501=
XM_011540040.1:c.4498C=	XP_011538342.1:p.Arg1500=
XM_011540041.1:c.4444C=	XP_011538343.1:p.Arg1482=
XM_011540042.1:c.4504C=	XP_011538344.1:p.Arg1502=
XM_011540043.1:c.4504C=	XP_011538345.1:p.Arg1502=
XM_011540044.1:c.4369C=	XP_011538346.1:p.Arg1457=
XM_011540045.1:c.4504C=	XP_011538347.1:p.Arg1502=
XM_011540046.1:c.3964C=	XP_011538348.1:p.Arg1322=
XM_011540047.1:c.3322C=	XP_011538349.1:p.Arg1108=
XM_011540048.1:c.4504C=	XP_011538350.1:p.Arg1502=
XM_011540049.1:c.4504C=	XP_011538351.1:p.Arg1502=
XM_011540050.1:c.4504C=	XP_011538352.1:p.Arg1502=
XM_011540051.1:c.4504C=	XP_011538353.1:p.Arg1502=
XM_011540052.1:c.832C=	XP_011538354.1:p.Arg278=
XM_011540053.1:c.4504C=	XP_011538355.1:p.Arg1502=
XR_945796.1:n.4747C=