Canonical Allele Identifier: CA1918874215

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793280A= , CM000672.2:g.71793280A=	GRCh38
NC_000010.10:g.73553037A= , CM000672.1:g.73553037A=	GRCh37
NC_000010.9:g.73223043A=	NCBI36
NG_008835.1:g.401334A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6352A= MANE Select	ENSP00000224721.9:p.Ile2118=
ENST00000224721.10:c.6367A=	ENSP00000224721.8:p.Ile2123=
ENST00000622827.4:c.6352A=	ENSP00000483211.1:p.Ile2118=
NM_022124.5:c.6352A=	NP_071407.4:p.Ile2118=
XM_006717940.2:c.6547A=	XP_006718003.1:p.Ile2183=
XM_006717942.2:c.6481A=	XP_006718005.1:p.Ile2161=
XM_011540039.1:c.6544A=	XP_011538341.1:p.Ile2182=
XM_011540040.1:c.6541A=	XP_011538342.1:p.Ile2181=
XM_011540041.1:c.6487A=	XP_011538343.1:p.Ile2163=
XM_011540042.1:c.6547A=	XP_011538344.1:p.Ile2183=
XM_011540043.1:c.6547A=	XP_011538345.1:p.Ile2183=
XM_011540044.1:c.6412A=	XP_011538346.1:p.Ile2138=
XM_011540045.1:c.6547A=	XP_011538347.1:p.Ile2183=
XM_011540046.1:c.6007A=	XP_011538348.1:p.Ile2003=
XM_011540047.1:c.5365A=	XP_011538349.1:p.Ile1789=
XM_011540048.1:c.6547A=	XP_011538350.1:p.Ile2183=
XM_011540049.1:c.6547A=	XP_011538351.1:p.Ile2183=
XM_011540050.1:c.6547A=	XP_011538352.1:p.Ile2183=
XM_011540051.1:c.6547A=	XP_011538353.1:p.Ile2183=
XM_011540052.1:c.2875A=	XP_011538354.1:p.Ile959=
XR_945796.1:n.6790A=
NM_022124.6:c.6352A= MANE Select	NP_071407.4:p.Ile2118=