Canonical Allele Identifier: CA1918874232

Gene: CDH23

Linked Data

• ClinVar Variation Id: 2833562
• ClinVar RCV Id: RCV003692039
• dbSNP Id: rs768035972

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793297G>A , CM000672.2:g.71793297G>A	GRCh38
NC_000010.10:g.73553054G>A , CM000672.1:g.73553054G>A	GRCh37
NC_000010.9:g.73223060G>A	NCBI36
NG_008835.1:g.401351G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6369G>A MANE Select	ENSP00000224721.9:p.Gly2123=
ENST00000224721.10:c.6384G>A	ENSP00000224721.8:p.Gly2128=
ENST00000622827.4:c.6369G>A	ENSP00000483211.1:p.Gly2123=
NM_022124.5:c.6369G>A	NP_071407.4:p.Gly2123=
XM_006717940.2:c.6564G>A	XP_006718003.1:p.Gly2188=
XM_006717942.2:c.6498G>A	XP_006718005.1:p.Gly2166=
XM_011540039.1:c.6561G>A	XP_011538341.1:p.Gly2187=
XM_011540040.1:c.6558G>A	XP_011538342.1:p.Gly2186=
XM_011540041.1:c.6504G>A	XP_011538343.1:p.Gly2168=
XM_011540042.1:c.6564G>A	XP_011538344.1:p.Gly2188=
XM_011540043.1:c.6564G>A	XP_011538345.1:p.Gly2188=
XM_011540044.1:c.6429G>A	XP_011538346.1:p.Gly2143=
XM_011540045.1:c.6564G>A	XP_011538347.1:p.Gly2188=
XM_011540046.1:c.6024G>A	XP_011538348.1:p.Gly2008=
XM_011540047.1:c.5382G>A	XP_011538349.1:p.Gly1794=
XM_011540048.1:c.6564G>A	XP_011538350.1:p.Gly2188=
XM_011540049.1:c.6564G>A	XP_011538351.1:p.Gly2188=
XM_011540050.1:c.6564G>A	XP_011538352.1:p.Gly2188=
XM_011540051.1:c.6564G>A	XP_011538353.1:p.Gly2188=
XM_011540052.1:c.2892G>A	XP_011538354.1:p.Gly964=
XR_945796.1:n.6807G>A
NM_022124.6:c.6369G>A MANE Select	NP_071407.4:p.Gly2123=