Canonical Allele Identifier: CA2838827956

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784982dup , CM000672.2:g.71784982dup	GRCh38
NC_000010.10:g.73544739dup , CM000672.1:g.73544739dup	GRCh37
NC_000010.9:g.73214745dup	NCBI36
NG_008835.1:g.393036dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5594dup MANE Select	ENSP00000224721.9:p.Val1866CysfsTer12
ENST00000224721.10:c.5609dup	ENSP00000224721.8:p.Val1871CysfsTer12
ENST00000622827.4:c.5594dup	ENSP00000483211.1:p.Val1866CysfsTer12
NM_022124.5:c.5594dup	NP_071407.4:p.Val1866CysfsTer12
XM_006717940.2:c.5789dup	XP_006718003.1:p.Val1931CysfsTer12
XM_006717942.2:c.5723dup	XP_006718005.1:p.Val1909CysfsTer12
XM_011540039.1:c.5786dup	XP_011538341.1:p.Val1930CysfsTer12
XM_011540040.1:c.5783dup	XP_011538342.1:p.Val1929CysfsTer12
XM_011540041.1:c.5729dup	XP_011538343.1:p.Val1911CysfsTer12
XM_011540042.1:c.5789dup	XP_011538344.1:p.Val1931CysfsTer12
XM_011540043.1:c.5789dup	XP_011538345.1:p.Val1931CysfsTer12
XM_011540044.1:c.5654dup	XP_011538346.1:p.Val1886CysfsTer12
XM_011540045.1:c.5789dup	XP_011538347.1:p.Val1931CysfsTer12
XM_011540046.1:c.5249dup	XP_011538348.1:p.Val1751CysfsTer12
XM_011540047.1:c.4607dup	XP_011538349.1:p.Val1537CysfsTer12
XM_011540048.1:c.5789dup	XP_011538350.1:p.Val1931CysfsTer12
XM_011540049.1:c.5789dup	XP_011538351.1:p.Val1931CysfsTer12
XM_011540050.1:c.5789dup	XP_011538352.1:p.Val1931CysfsTer12
XM_011540051.1:c.5789dup	XP_011538353.1:p.Val1931CysfsTer12
XM_011540052.1:c.2117dup	XP_011538354.1:p.Val707CysfsTer12
XM_011540053.1:c.5789dup	XP_011538355.1:p.Val1931CysfsTer12
XR_945796.1:n.6032dup
NM_022124.6:c.5594dup MANE Select	NP_071407.4:p.Val1866CysfsTer12