Canonical Allele Identifier: CA1918874179

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793251T= , CM000672.2:g.71793251T=	GRCh38
NC_000010.10:g.73553008T= , CM000672.1:g.73553008T=	GRCh37
NC_000010.9:g.73223014T=	NCBI36
NG_008835.1:g.401305T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6323T= MANE Select	ENSP00000224721.9:p.Ile2108=
ENST00000224721.10:c.6338T=	ENSP00000224721.8:p.Ile2113=
ENST00000622827.4:c.6323T=	ENSP00000483211.1:p.Ile2108=
NM_022124.5:c.6323T=	NP_071407.4:p.Ile2108=
XM_006717940.2:c.6518T=	XP_006718003.1:p.Ile2173=
XM_006717942.2:c.6452T=	XP_006718005.1:p.Ile2151=
XM_011540039.1:c.6515T=	XP_011538341.1:p.Ile2172=
XM_011540040.1:c.6512T=	XP_011538342.1:p.Ile2171=
XM_011540041.1:c.6458T=	XP_011538343.1:p.Ile2153=
XM_011540042.1:c.6518T=	XP_011538344.1:p.Ile2173=
XM_011540043.1:c.6518T=	XP_011538345.1:p.Ile2173=
XM_011540044.1:c.6383T=	XP_011538346.1:p.Ile2128=
XM_011540045.1:c.6518T=	XP_011538347.1:p.Ile2173=
XM_011540046.1:c.5978T=	XP_011538348.1:p.Ile1993=
XM_011540047.1:c.5336T=	XP_011538349.1:p.Ile1779=
XM_011540048.1:c.6518T=	XP_011538350.1:p.Ile2173=
XM_011540049.1:c.6518T=	XP_011538351.1:p.Ile2173=
XM_011540050.1:c.6518T=	XP_011538352.1:p.Ile2173=
XM_011540051.1:c.6518T=	XP_011538353.1:p.Ile2173=
XM_011540052.1:c.2846T=	XP_011538354.1:p.Ile949=
XR_945796.1:n.6761T=
NM_022124.6:c.6323T= MANE Select	NP_071407.4:p.Ile2108=