Canonical Allele Identifier: CA470060690

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544662C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784905C>A , CM000672.2:g.71784905C>A	GRCh38
NC_000010.10:g.73544662C>A , CM000672.1:g.73544662C>A	GRCh37
NC_000010.9:g.73214668C>A	NCBI36
NG_008835.1:g.392959C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5517C>A MANE Select	ENSP00000224721.9:p.Ile1839=
ENST00000224721.10:c.5532C>A	ENSP00000224721.8:p.Ile1844=
ENST00000622827.4:c.5517C>A	ENSP00000483211.1:p.Ile1839=
NM_022124.5:c.5517C>A	NP_071407.4:p.Ile1839=
XM_006717940.2:c.5712C>A	XP_006718003.1:p.Ile1904=
XM_006717942.2:c.5646C>A	XP_006718005.1:p.Ile1882=
XM_011540039.1:c.5709C>A	XP_011538341.1:p.Ile1903=
XM_011540040.1:c.5706C>A	XP_011538342.1:p.Ile1902=
XM_011540041.1:c.5652C>A	XP_011538343.1:p.Ile1884=
XM_011540042.1:c.5712C>A	XP_011538344.1:p.Ile1904=
XM_011540043.1:c.5712C>A	XP_011538345.1:p.Ile1904=
XM_011540044.1:c.5577C>A	XP_011538346.1:p.Ile1859=
XM_011540045.1:c.5712C>A	XP_011538347.1:p.Ile1904=
XM_011540046.1:c.5172C>A	XP_011538348.1:p.Ile1724=
XM_011540047.1:c.4530C>A	XP_011538349.1:p.Ile1510=
XM_011540048.1:c.5712C>A	XP_011538350.1:p.Ile1904=
XM_011540049.1:c.5712C>A	XP_011538351.1:p.Ile1904=
XM_011540050.1:c.5712C>A	XP_011538352.1:p.Ile1904=
XM_011540051.1:c.5712C>A	XP_011538353.1:p.Ile1904=
XM_011540052.1:c.2040C>A	XP_011538354.1:p.Ile680=
XM_011540053.1:c.5712C>A	XP_011538355.1:p.Ile1904=
XR_945796.1:n.5955C>A
NM_022124.6:c.5517C>A MANE Select	NP_071407.4:p.Ile1839=