Canonical Allele Identifier: CA1918862478

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785051T= , CM000672.2:g.71785051T=	GRCh38
NC_000010.10:g.73544808T= , CM000672.1:g.73544808T=	GRCh37
NC_000010.9:g.73214814T=	NCBI36
NG_008835.1:g.393105T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5663T= MANE Select	ENSP00000224721.9:p.Phe1888=
ENST00000224721.10:c.5678T=	ENSP00000224721.8:p.Phe1893=
ENST00000622827.4:c.5663T=	ENSP00000483211.1:p.Phe1888=
NM_022124.5:c.5663T=	NP_071407.4:p.Phe1888=
XM_006717940.2:c.5858T=	XP_006718003.1:p.Phe1953=
XM_006717942.2:c.5792T=	XP_006718005.1:p.Phe1931=
XM_011540039.1:c.5855T=	XP_011538341.1:p.Phe1952=
XM_011540040.1:c.5852T=	XP_011538342.1:p.Phe1951=
XM_011540041.1:c.5798T=	XP_011538343.1:p.Phe1933=
XM_011540042.1:c.5858T=	XP_011538344.1:p.Phe1953=
XM_011540043.1:c.5858T=	XP_011538345.1:p.Phe1953=
XM_011540044.1:c.5723T=	XP_011538346.1:p.Phe1908=
XM_011540045.1:c.5858T=	XP_011538347.1:p.Phe1953=
XM_011540046.1:c.5318T=	XP_011538348.1:p.Phe1773=
XM_011540047.1:c.4676T=	XP_011538349.1:p.Phe1559=
XM_011540048.1:c.5858T=	XP_011538350.1:p.Phe1953=
XM_011540049.1:c.5858T=	XP_011538351.1:p.Phe1953=
XM_011540050.1:c.5858T=	XP_011538352.1:p.Phe1953=
XM_011540051.1:c.5858T=	XP_011538353.1:p.Phe1953=
XM_011540052.1:c.2186T=	XP_011538354.1:p.Phe729=
XM_011540053.1:c.5858T=	XP_011538355.1:p.Phe1953=
XR_945796.1:n.6101T=
NM_022124.6:c.5663T= MANE Select	NP_071407.4:p.Phe1888=