Canonical Allele Identifier: CA137446

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71777692G>A , CM000672.2:g.71777692G>A	GRCh38
NC_000010.10:g.73537449G>A , CM000672.1:g.73537449G>A	GRCh37
NC_000010.9:g.73207455G>A	NCBI36
NG_008835.1:g.385746G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4858G>A MANE Select	ENSP00000224721.9:p.Val1620Met
ENST00000224721.10:c.4873G>A	ENSP00000224721.8:p.Val1625Met
ENST00000622827.4:c.4858G>A	ENSP00000483211.1:p.Val1620Met
NM_022124.5:c.4858G>A	NP_071407.4:p.Val1620Met
XM_006717940.2:c.5053G>A	XP_006718003.1:p.Val1685Met
XM_006717942.2:c.4987G>A	XP_006718005.1:p.Val1663Met
XM_011540039.1:c.5050G>A	XP_011538341.1:p.Val1684Met
XM_011540040.1:c.5047G>A	XP_011538342.1:p.Val1683Met
XM_011540041.1:c.4993G>A	XP_011538343.1:p.Val1665Met
XM_011540042.1:c.5053G>A	XP_011538344.1:p.Val1685Met
XM_011540043.1:c.5053G>A	XP_011538345.1:p.Val1685Met
XM_011540044.1:c.4918G>A	XP_011538346.1:p.Val1640Met
XM_011540045.1:c.5053G>A	XP_011538347.1:p.Val1685Met
XM_011540046.1:c.4513G>A	XP_011538348.1:p.Val1505Met
XM_011540047.1:c.3871G>A	XP_011538349.1:p.Val1291Met
XM_011540048.1:c.5053G>A	XP_011538350.1:p.Val1685Met
XM_011540049.1:c.5053G>A	XP_011538351.1:p.Val1685Met
XM_011540050.1:c.5053G>A	XP_011538352.1:p.Val1685Met
XM_011540051.1:c.5053G>A	XP_011538353.1:p.Val1685Met
XM_011540052.1:c.1381G>A	XP_011538354.1:p.Val461Met
XM_011540053.1:c.5053G>A	XP_011538355.1:p.Val1685Met
XR_945796.1:n.5296G>A
NM_022124.6:c.4858G>A MANE Select	NP_071407.4:p.Val1620Met