Canonical Allele Identifier: CA1918861949

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784865_71784868delinsCCCT , CM000672.2:g.71784865_71784868delinsCCCT	GRCh38
NC_000010.10:g.73544622_73544625delinsCCCT , CM000672.1:g.73544622_73544625delinsCCCT	GRCh37
NC_000010.9:g.73214628_73214631delinsCCCT	NCBI36
NG_008835.1:g.392919_392922delinsCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5503-26_5503-23delinsCCCT MANE Select	ENSP00000224721.9:n.5503-26_5503-23delinsCCCT
ENST00000224721.10:c.5518-26_5518-23delinsCCCT	ENSP00000224721.8:n.5518-26_5518-23delinsCCCT
ENST00000622827.4:c.5503-26_5503-23delinsCCCT	ENSP00000483211.1:n.5503-26_5503-23delinsCCCT
NM_022124.5:c.5503-26_5503-23delinsCCCT	NP_071407.4:n.5503-26_5503-23delinsCCCT
XM_006717940.2:c.5698-26_5698-23delinsCCCT	XP_006718003.1:n.5698-26_5698-23delinsCCCT
XM_006717942.2:c.5632-26_5632-23delinsCCCT	XP_006718005.1:n.5632-26_5632-23delinsCCCT
XM_011540039.1:c.5695-26_5695-23delinsCCCT	XP_011538341.1:n.5695-26_5695-23delinsCCCT
XM_011540040.1:c.5692-26_5692-23delinsCCCT	XP_011538342.1:n.5692-26_5692-23delinsCCCT
XM_011540041.1:c.5638-26_5638-23delinsCCCT	XP_011538343.1:n.5638-26_5638-23delinsCCCT
XM_011540042.1:c.5698-26_5698-23delinsCCCT	XP_011538344.1:n.5698-26_5698-23delinsCCCT
XM_011540043.1:c.5698-26_5698-23delinsCCCT	XP_011538345.1:n.5698-26_5698-23delinsCCCT
XM_011540044.1:c.5563-26_5563-23delinsCCCT	XP_011538346.1:n.5563-26_5563-23delinsCCCT
XM_011540045.1:c.5698-26_5698-23delinsCCCT	XP_011538347.1:n.5698-26_5698-23delinsCCCT
XM_011540046.1:c.5158-26_5158-23delinsCCCT	XP_011538348.1:n.5158-26_5158-23delinsCCCT
XM_011540047.1:c.4516-26_4516-23delinsCCCT	XP_011538349.1:n.4516-26_4516-23delinsCCCT
XM_011540048.1:c.5698-26_5698-23delinsCCCT	XP_011538350.1:n.5698-26_5698-23delinsCCCT
XM_011540049.1:c.5698-26_5698-23delinsCCCT	XP_011538351.1:n.5698-26_5698-23delinsCCCT
XM_011540050.1:c.5698-26_5698-23delinsCCCT	XP_011538352.1:n.5698-26_5698-23delinsCCCT
XM_011540051.1:c.5698-26_5698-23delinsCCCT	XP_011538353.1:n.5698-26_5698-23delinsCCCT
XM_011540052.1:c.2026-26_2026-23delinsCCCT	XP_011538354.1:n.2026-26_2026-23delinsCCCT
XM_011540053.1:c.5698-26_5698-23delinsCCCT	XP_011538355.1:n.5698-26_5698-23delinsCCCT
XR_945796.1:n.5941-26_5941-23delinsCCCT
NM_022124.6:c.5503-26_5503-23delinsCCCT MANE Select	NP_071407.4:n.5503-26_5503-23delinsCCCT