Canonical Allele Identifier: CA1918862572

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785070C= , CM000672.2:g.71785070C=	GRCh38
NC_000010.10:g.73544827C= , CM000672.1:g.73544827C=	GRCh37
NC_000010.9:g.73214833C=	NCBI36
NG_008835.1:g.393124C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5682C= MANE Select	ENSP00000224721.9:p.Asn1894=
ENST00000224721.10:c.5697C=	ENSP00000224721.8:p.Asn1899=
ENST00000622827.4:c.5682C=	ENSP00000483211.1:p.Asn1894=
NM_022124.5:c.5682C=	NP_071407.4:p.Asn1894=
XM_006717940.2:c.5877C=	XP_006718003.1:p.Asn1959=
XM_006717942.2:c.5811C=	XP_006718005.1:p.Asn1937=
XM_011540039.1:c.5874C=	XP_011538341.1:p.Asn1958=
XM_011540040.1:c.5871C=	XP_011538342.1:p.Asn1957=
XM_011540041.1:c.5817C=	XP_011538343.1:p.Asn1939=
XM_011540042.1:c.5877C=	XP_011538344.1:p.Asn1959=
XM_011540043.1:c.5877C=	XP_011538345.1:p.Asn1959=
XM_011540044.1:c.5742C=	XP_011538346.1:p.Asn1914=
XM_011540045.1:c.5877C=	XP_011538347.1:p.Asn1959=
XM_011540046.1:c.5337C=	XP_011538348.1:p.Asn1779=
XM_011540047.1:c.4695C=	XP_011538349.1:p.Asn1565=
XM_011540048.1:c.5877C=	XP_011538350.1:p.Asn1959=
XM_011540049.1:c.5877C=	XP_011538351.1:p.Asn1959=
XM_011540050.1:c.5877C=	XP_011538352.1:p.Asn1959=
XM_011540051.1:c.5877C=	XP_011538353.1:p.Asn1959=
XM_011540052.1:c.2205C=	XP_011538354.1:p.Asn735=
XM_011540053.1:c.5877C=	XP_011538355.1:p.Asn1959=
XR_945796.1:n.6120C=
NM_022124.6:c.5682C= MANE Select	NP_071407.4:p.Asn1894=