Canonical Allele Identifier: CA1918853859

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740900A= , CM000672.2:g.71740900A=	GRCh38
NC_000010.10:g.73500657A= , CM000672.1:g.73500657A=	GRCh37
NC_000010.9:g.73170663A=	NCBI36
NG_008835.1:g.348954A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4567A= MANE Select	ENSP00000224721.9:p.Asn1523=
ENST00000224721.10:c.4582A=	ENSP00000224721.8:p.Asn1528=
ENST00000398792.3:n.1256A=
ENST00000622827.4:c.4567A=	ENSP00000483211.1:p.Asn1523=
NM_022124.5:c.4567A=	NP_071407.4:p.Asn1523=
XM_006717940.2:c.4762A=	XP_006718003.1:p.Asn1588=
XM_006717942.2:c.4696A=	XP_006718005.1:p.Asn1566=
XM_011540039.1:c.4759A=	XP_011538341.1:p.Asn1587=
XM_011540040.1:c.4756A=	XP_011538342.1:p.Asn1586=
XM_011540041.1:c.4702A=	XP_011538343.1:p.Asn1568=
XM_011540042.1:c.4762A=	XP_011538344.1:p.Asn1588=
XM_011540043.1:c.4762A=	XP_011538345.1:p.Asn1588=
XM_011540044.1:c.4627A=	XP_011538346.1:p.Asn1543=
XM_011540045.1:c.4762A=	XP_011538347.1:p.Asn1588=
XM_011540046.1:c.4222A=	XP_011538348.1:p.Asn1408=
XM_011540047.1:c.3580A=	XP_011538349.1:p.Asn1194=
XM_011540048.1:c.4762A=	XP_011538350.1:p.Asn1588=
XM_011540049.1:c.4762A=	XP_011538351.1:p.Asn1588=
XM_011540050.1:c.4762A=	XP_011538352.1:p.Asn1588=
XM_011540051.1:c.4762A=	XP_011538353.1:p.Asn1588=
XM_011540052.1:c.1090A=	XP_011538354.1:p.Asn364=
XM_011540053.1:c.4762A=	XP_011538355.1:p.Asn1588=
XR_945796.1:n.5005A=
NM_022124.6:c.4567A= MANE Select	NP_071407.4:p.Asn1523=