Canonical Allele Identifier: CA1918853866

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740915G= , CM000672.2:g.71740915G=	GRCh38
NC_000010.10:g.73500672G= , CM000672.1:g.73500672G=	GRCh37
NC_000010.9:g.73170678G=	NCBI36
NG_008835.1:g.348969G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4582G= MANE Select	ENSP00000224721.9:p.Glu1528=
ENST00000224721.10:c.4597G=	ENSP00000224721.8:p.Glu1533=
ENST00000398792.3:n.1271G=
ENST00000622827.4:c.4582G=	ENSP00000483211.1:p.Glu1528=
NM_022124.5:c.4582G=	NP_071407.4:p.Glu1528=
XM_006717940.2:c.4777G=	XP_006718003.1:p.Glu1593=
XM_006717942.2:c.4711G=	XP_006718005.1:p.Glu1571=
XM_011540039.1:c.4774G=	XP_011538341.1:p.Glu1592=
XM_011540040.1:c.4771G=	XP_011538342.1:p.Glu1591=
XM_011540041.1:c.4717G=	XP_011538343.1:p.Glu1573=
XM_011540042.1:c.4777G=	XP_011538344.1:p.Glu1593=
XM_011540043.1:c.4777G=	XP_011538345.1:p.Glu1593=
XM_011540044.1:c.4642G=	XP_011538346.1:p.Glu1548=
XM_011540045.1:c.4777G=	XP_011538347.1:p.Glu1593=
XM_011540046.1:c.4237G=	XP_011538348.1:p.Glu1413=
XM_011540047.1:c.3595G=	XP_011538349.1:p.Glu1199=
XM_011540048.1:c.4777G=	XP_011538350.1:p.Glu1593=
XM_011540049.1:c.4777G=	XP_011538351.1:p.Glu1593=
XM_011540050.1:c.4777G=	XP_011538352.1:p.Glu1593=
XM_011540051.1:c.4777G=	XP_011538353.1:p.Glu1593=
XM_011540052.1:c.1105G=	XP_011538354.1:p.Glu369=
XM_011540053.1:c.4777G=	XP_011538355.1:p.Glu1593=
XR_945796.1:n.5020G=
NM_022124.6:c.4582G= MANE Select	NP_071407.4:p.Glu1528=