Canonical Allele Identifier: CA1918853826

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740834G= , CM000672.2:g.71740834G=	GRCh38
NC_000010.10:g.73500591G= , CM000672.1:g.73500591G=	GRCh37
NC_000010.9:g.73170597G=	NCBI36
NG_008835.1:g.348888G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4501G= MANE Select	ENSP00000224721.9:p.Asp1501=
ENST00000224721.10:c.4516G=	ENSP00000224721.8:p.Asp1506=
ENST00000398792.3:n.1190G=
ENST00000622827.4:c.4501G=	ENSP00000483211.1:p.Asp1501=
NM_022124.5:c.4501G=	NP_071407.4:p.Asp1501=
XM_006717940.2:c.4696G=	XP_006718003.1:p.Asp1566=
XM_006717942.2:c.4630G=	XP_006718005.1:p.Asp1544=
XM_011540039.1:c.4693G=	XP_011538341.1:p.Asp1565=
XM_011540040.1:c.4690G=	XP_011538342.1:p.Asp1564=
XM_011540041.1:c.4636G=	XP_011538343.1:p.Asp1546=
XM_011540042.1:c.4696G=	XP_011538344.1:p.Asp1566=
XM_011540043.1:c.4696G=	XP_011538345.1:p.Asp1566=
XM_011540044.1:c.4561G=	XP_011538346.1:p.Asp1521=
XM_011540045.1:c.4696G=	XP_011538347.1:p.Asp1566=
XM_011540046.1:c.4156G=	XP_011538348.1:p.Asp1386=
XM_011540047.1:c.3514G=	XP_011538349.1:p.Asp1172=
XM_011540048.1:c.4696G=	XP_011538350.1:p.Asp1566=
XM_011540049.1:c.4696G=	XP_011538351.1:p.Asp1566=
XM_011540050.1:c.4696G=	XP_011538352.1:p.Asp1566=
XM_011540051.1:c.4696G=	XP_011538353.1:p.Asp1566=
XM_011540052.1:c.1024G=	XP_011538354.1:p.Asp342=
XM_011540053.1:c.4696G=	XP_011538355.1:p.Asp1566=
XR_945796.1:n.4939G=
NM_022124.6:c.4501G= MANE Select	NP_071407.4:p.Asp1501=