Canonical Allele Identifier: CA1918875444

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71779351C= , CM000672.2:g.71779351C=	GRCh38
NC_000010.10:g.73539108C= , CM000672.1:g.73539108C=	GRCh37
NC_000010.9:g.73209114C=	NCBI36
NG_008835.1:g.387405C=

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.5272C= MANE Select	NP_071407.4:p.Gln1758=
ENST00000224721.12:c.5272C= MANE Select	ENSP00000224721.9:p.Gln1758=
NM_022124.5:c.5272C=	NP_071407.4:p.Gln1758=
ENST00000224721.10:c.5287C=	ENSP00000224721.8:p.Gln1763=
ENST00000622827.4:c.5272C=	ENSP00000483211.1:p.Gln1758=
XM_006717940.2:c.5467C=	XP_006718003.1:p.Gln1823=
XM_006717942.2:c.5401C=	XP_006718005.1:p.Gln1801=
XM_011540039.1:c.5464C=	XP_011538341.1:p.Gln1822=
XM_011540040.1:c.5461C=	XP_011538342.1:p.Gln1821=
XM_011540041.1:c.5407C=	XP_011538343.1:p.Gln1803=
XM_011540042.1:c.5467C=	XP_011538344.1:p.Gln1823=
XM_011540043.1:c.5467C=	XP_011538345.1:p.Gln1823=
XM_011540044.1:c.5332C=	XP_011538346.1:p.Gln1778=
XM_011540045.1:c.5467C=	XP_011538347.1:p.Gln1823=
XM_011540046.1:c.4927C=	XP_011538348.1:p.Gln1643=
XM_011540047.1:c.4285C=	XP_011538349.1:p.Gln1429=
XM_011540048.1:c.5467C=	XP_011538350.1:p.Gln1823=
XM_011540049.1:c.5467C=	XP_011538351.1:p.Gln1823=
XM_011540050.1:c.5467C=	XP_011538352.1:p.Gln1823=
XM_011540051.1:c.5467C=	XP_011538353.1:p.Gln1823=
XM_011540052.1:c.1795C=	XP_011538354.1:p.Gln599=
XM_011540053.1:c.5467C=	XP_011538355.1:p.Gln1823=
XR_945796.1:n.5710C=