Canonical Allele Identifier: CA1918853861

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740903C= , CM000672.2:g.71740903C=	GRCh38
NC_000010.10:g.73500660C= , CM000672.1:g.73500660C=	GRCh37
NC_000010.9:g.73170666C=	NCBI36
NG_008835.1:g.348957C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4570C= MANE Select	ENSP00000224721.9:p.Pro1524=
ENST00000224721.10:c.4585C=	ENSP00000224721.8:p.Pro1529=
ENST00000398792.3:n.1259C=
ENST00000622827.4:c.4570C=	ENSP00000483211.1:p.Pro1524=
NM_022124.5:c.4570C=	NP_071407.4:p.Pro1524=
XM_006717940.2:c.4765C=	XP_006718003.1:p.Pro1589=
XM_006717942.2:c.4699C=	XP_006718005.1:p.Pro1567=
XM_011540039.1:c.4762C=	XP_011538341.1:p.Pro1588=
XM_011540040.1:c.4759C=	XP_011538342.1:p.Pro1587=
XM_011540041.1:c.4705C=	XP_011538343.1:p.Pro1569=
XM_011540042.1:c.4765C=	XP_011538344.1:p.Pro1589=
XM_011540043.1:c.4765C=	XP_011538345.1:p.Pro1589=
XM_011540044.1:c.4630C=	XP_011538346.1:p.Pro1544=
XM_011540045.1:c.4765C=	XP_011538347.1:p.Pro1589=
XM_011540046.1:c.4225C=	XP_011538348.1:p.Pro1409=
XM_011540047.1:c.3583C=	XP_011538349.1:p.Pro1195=
XM_011540048.1:c.4765C=	XP_011538350.1:p.Pro1589=
XM_011540049.1:c.4765C=	XP_011538351.1:p.Pro1589=
XM_011540050.1:c.4765C=	XP_011538352.1:p.Pro1589=
XM_011540051.1:c.4765C=	XP_011538353.1:p.Pro1589=
XM_011540052.1:c.1093C=	XP_011538354.1:p.Pro365=
XM_011540053.1:c.4765C=	XP_011538355.1:p.Pro1589=
XR_945796.1:n.5008C=
NM_022124.6:c.4570C= MANE Select	NP_071407.4:p.Pro1524=