Canonical Allele Identifier: CA1918862428

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785036A= , CM000672.2:g.71785036A=	GRCh38
NC_000010.10:g.73544793A= , CM000672.1:g.73544793A=	GRCh37
NC_000010.9:g.73214799A=	NCBI36
NG_008835.1:g.393090A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5648A= MANE Select	ENSP00000224721.9:p.Asn1883=
ENST00000224721.10:c.5663A=	ENSP00000224721.8:p.Asn1888=
ENST00000622827.4:c.5648A=	ENSP00000483211.1:p.Asn1883=
NM_022124.5:c.5648A=	NP_071407.4:p.Asn1883=
XM_006717940.2:c.5843A=	XP_006718003.1:p.Asn1948=
XM_006717942.2:c.5777A=	XP_006718005.1:p.Asn1926=
XM_011540039.1:c.5840A=	XP_011538341.1:p.Asn1947=
XM_011540040.1:c.5837A=	XP_011538342.1:p.Asn1946=
XM_011540041.1:c.5783A=	XP_011538343.1:p.Asn1928=
XM_011540042.1:c.5843A=	XP_011538344.1:p.Asn1948=
XM_011540043.1:c.5843A=	XP_011538345.1:p.Asn1948=
XM_011540044.1:c.5708A=	XP_011538346.1:p.Asn1903=
XM_011540045.1:c.5843A=	XP_011538347.1:p.Asn1948=
XM_011540046.1:c.5303A=	XP_011538348.1:p.Asn1768=
XM_011540047.1:c.4661A=	XP_011538349.1:p.Asn1554=
XM_011540048.1:c.5843A=	XP_011538350.1:p.Asn1948=
XM_011540049.1:c.5843A=	XP_011538351.1:p.Asn1948=
XM_011540050.1:c.5843A=	XP_011538352.1:p.Asn1948=
XM_011540051.1:c.5843A=	XP_011538353.1:p.Asn1948=
XM_011540052.1:c.2171A=	XP_011538354.1:p.Asn724=
XM_011540053.1:c.5843A=	XP_011538355.1:p.Asn1948=
XR_945796.1:n.6086A=
NM_022124.6:c.5648A= MANE Select	NP_071407.4:p.Asn1883=