Canonical Allele Identifier: CA1918874212

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793276C= , CM000672.2:g.71793276C=	GRCh38
NC_000010.10:g.73553033C= , CM000672.1:g.73553033C=	GRCh37
NC_000010.9:g.73223039C=	NCBI36
NG_008835.1:g.401330C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6348C= MANE Select	ENSP00000224721.9:p.Phe2116=
ENST00000224721.10:c.6363C=	ENSP00000224721.8:p.Phe2121=
ENST00000622827.4:c.6348C=	ENSP00000483211.1:p.Phe2116=
NM_022124.5:c.6348C=	NP_071407.4:p.Phe2116=
XM_006717940.2:c.6543C=	XP_006718003.1:p.Phe2181=
XM_006717942.2:c.6477C=	XP_006718005.1:p.Phe2159=
XM_011540039.1:c.6540C=	XP_011538341.1:p.Phe2180=
XM_011540040.1:c.6537C=	XP_011538342.1:p.Phe2179=
XM_011540041.1:c.6483C=	XP_011538343.1:p.Phe2161=
XM_011540042.1:c.6543C=	XP_011538344.1:p.Phe2181=
XM_011540043.1:c.6543C=	XP_011538345.1:p.Phe2181=
XM_011540044.1:c.6408C=	XP_011538346.1:p.Phe2136=
XM_011540045.1:c.6543C=	XP_011538347.1:p.Phe2181=
XM_011540046.1:c.6003C=	XP_011538348.1:p.Phe2001=
XM_011540047.1:c.5361C=	XP_011538349.1:p.Phe1787=
XM_011540048.1:c.6543C=	XP_011538350.1:p.Phe2181=
XM_011540049.1:c.6543C=	XP_011538351.1:p.Phe2181=
XM_011540050.1:c.6543C=	XP_011538352.1:p.Phe2181=
XM_011540051.1:c.6543C=	XP_011538353.1:p.Phe2181=
XM_011540052.1:c.2871C=	XP_011538354.1:p.Phe957=
XR_945796.1:n.6786C=
NM_022124.6:c.6348C= MANE Select	NP_071407.4:p.Phe2116=