Canonical Allele Identifier: CA175500

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71791173G>A , CM000672.2:g.71791173G>A	GRCh38
NC_000010.10:g.73550930G>A , CM000672.1:g.73550930G>A	GRCh37
NC_000010.9:g.73220936G>A	NCBI36
NG_008835.1:g.399227G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6091G>A MANE Select	ENSP00000224721.9:p.Ala2031Thr
ENST00000224721.10:c.6106G>A	ENSP00000224721.8:p.Ala2036Thr
ENST00000622827.4:c.6091G>A	ENSP00000483211.1:p.Ala2031Thr
NM_022124.5:c.6091G>A	NP_071407.4:p.Ala2031Thr
XM_006717940.2:c.6286G>A	XP_006718003.1:p.Ala2096Thr
XM_006717942.2:c.6220G>A	XP_006718005.1:p.Ala2074Thr
XM_011540039.1:c.6283G>A	XP_011538341.1:p.Ala2095Thr
XM_011540040.1:c.6280G>A	XP_011538342.1:p.Ala2094Thr
XM_011540041.1:c.6226G>A	XP_011538343.1:p.Ala2076Thr
XM_011540042.1:c.6286G>A	XP_011538344.1:p.Ala2096Thr
XM_011540043.1:c.6286G>A	XP_011538345.1:p.Ala2096Thr
XM_011540044.1:c.6151G>A	XP_011538346.1:p.Ala2051Thr
XM_011540045.1:c.6286G>A	XP_011538347.1:p.Ala2096Thr
XM_011540046.1:c.5746G>A	XP_011538348.1:p.Ala1916Thr
XM_011540047.1:c.5104G>A	XP_011538349.1:p.Ala1702Thr
XM_011540048.1:c.6286G>A	XP_011538350.1:p.Ala2096Thr
XM_011540049.1:c.6286G>A	XP_011538351.1:p.Ala2096Thr
XM_011540050.1:c.6286G>A	XP_011538352.1:p.Ala2096Thr
XM_011540051.1:c.6286G>A	XP_011538353.1:p.Ala2096Thr
XM_011540052.1:c.2614G>A	XP_011538354.1:p.Ala872Thr
XR_945796.1:n.6529G>A
NM_022124.6:c.6091G>A MANE Select	NP_071407.4:p.Ala2031Thr