Canonical Allele Identifier: CA1918862512

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785056A= , CM000672.2:g.71785056A=	GRCh38
NC_000010.10:g.73544813A= , CM000672.1:g.73544813A=	GRCh37
NC_000010.9:g.73214819A=	NCBI36
NG_008835.1:g.393110A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5668A= MANE Select	ENSP00000224721.9:p.Ile1890=
ENST00000224721.10:c.5683A=	ENSP00000224721.8:p.Ile1895=
ENST00000622827.4:c.5668A=	ENSP00000483211.1:p.Ile1890=
NM_022124.5:c.5668A=	NP_071407.4:p.Ile1890=
XM_006717940.2:c.5863A=	XP_006718003.1:p.Ile1955=
XM_006717942.2:c.5797A=	XP_006718005.1:p.Ile1933=
XM_011540039.1:c.5860A=	XP_011538341.1:p.Ile1954=
XM_011540040.1:c.5857A=	XP_011538342.1:p.Ile1953=
XM_011540041.1:c.5803A=	XP_011538343.1:p.Ile1935=
XM_011540042.1:c.5863A=	XP_011538344.1:p.Ile1955=
XM_011540043.1:c.5863A=	XP_011538345.1:p.Ile1955=
XM_011540044.1:c.5728A=	XP_011538346.1:p.Ile1910=
XM_011540045.1:c.5863A=	XP_011538347.1:p.Ile1955=
XM_011540046.1:c.5323A=	XP_011538348.1:p.Ile1775=
XM_011540047.1:c.4681A=	XP_011538349.1:p.Ile1561=
XM_011540048.1:c.5863A=	XP_011538350.1:p.Ile1955=
XM_011540049.1:c.5863A=	XP_011538351.1:p.Ile1955=
XM_011540050.1:c.5863A=	XP_011538352.1:p.Ile1955=
XM_011540051.1:c.5863A=	XP_011538353.1:p.Ile1955=
XM_011540052.1:c.2191A=	XP_011538354.1:p.Ile731=
XM_011540053.1:c.5863A=	XP_011538355.1:p.Ile1955=
XR_945796.1:n.6106A=
NM_022124.6:c.5668A= MANE Select	NP_071407.4:p.Ile1890=