Canonical Allele Identifier: CA1918861764

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784768_71784774delinsTTCTCCA , CM000672.2:g.71784768_71784774delinsTTCTCCA	GRCh38
NC_000010.10:g.73544525_73544531delinsTTCTCCA , CM000672.1:g.73544525_73544531delinsTTCTCCA	GRCh37
NC_000010.9:g.73214531_73214537delinsTTCTCCA	NCBI36
NG_008835.1:g.392822_392828delinsTTCTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5503-123_5503-117delinsTTCTCCA MANE Select	ENSP00000224721.9:n.5503-123_5503-117delinsTTCTCCA
ENST00000224721.10:c.5518-123_5518-117delinsTTCTCCA	ENSP00000224721.8:n.5518-123_5518-117delinsTTCTCCA
ENST00000622827.4:c.5503-123_5503-117delinsTTCTCCA	ENSP00000483211.1:n.5503-123_5503-117delinsTTCTCCA
NM_022124.5:c.5503-123_5503-117delinsTTCTCCA	NP_071407.4:n.5503-123_5503-117delinsTTCTCCA
XM_006717940.2:c.5698-123_5698-117delinsTTCTCCA	XP_006718003.1:n.5698-123_5698-117delinsTTCTCCA
XM_006717942.2:c.5632-123_5632-117delinsTTCTCCA	XP_006718005.1:n.5632-123_5632-117delinsTTCTCCA
XM_011540039.1:c.5695-123_5695-117delinsTTCTCCA	XP_011538341.1:n.5695-123_5695-117delinsTTCTCCA
XM_011540040.1:c.5692-123_5692-117delinsTTCTCCA	XP_011538342.1:n.5692-123_5692-117delinsTTCTCCA
XM_011540041.1:c.5638-123_5638-117delinsTTCTCCA	XP_011538343.1:n.5638-123_5638-117delinsTTCTCCA
XM_011540042.1:c.5698-123_5698-117delinsTTCTCCA	XP_011538344.1:n.5698-123_5698-117delinsTTCTCCA
XM_011540043.1:c.5698-123_5698-117delinsTTCTCCA	XP_011538345.1:n.5698-123_5698-117delinsTTCTCCA
XM_011540044.1:c.5563-123_5563-117delinsTTCTCCA	XP_011538346.1:n.5563-123_5563-117delinsTTCTCCA
XM_011540045.1:c.5698-123_5698-117delinsTTCTCCA	XP_011538347.1:n.5698-123_5698-117delinsTTCTCCA
XM_011540046.1:c.5158-123_5158-117delinsTTCTCCA	XP_011538348.1:n.5158-123_5158-117delinsTTCTCCA
XM_011540047.1:c.4516-123_4516-117delinsTTCTCCA	XP_011538349.1:n.4516-123_4516-117delinsTTCTCCA
XM_011540048.1:c.5698-123_5698-117delinsTTCTCCA	XP_011538350.1:n.5698-123_5698-117delinsTTCTCCA
XM_011540049.1:c.5698-123_5698-117delinsTTCTCCA	XP_011538351.1:n.5698-123_5698-117delinsTTCTCCA
XM_011540050.1:c.5698-123_5698-117delinsTTCTCCA	XP_011538352.1:n.5698-123_5698-117delinsTTCTCCA
XM_011540051.1:c.5698-123_5698-117delinsTTCTCCA	XP_011538353.1:n.5698-123_5698-117delinsTTCTCCA
XM_011540052.1:c.2026-123_2026-117delinsTTCTCCA	XP_011538354.1:n.2026-123_2026-117delinsTTCTCCA
XM_011540053.1:c.5698-123_5698-117delinsTTCTCCA	XP_011538355.1:n.5698-123_5698-117delinsTTCTCCA
XR_945796.1:n.5941-123_5941-117delinsTTCTCCA
NM_022124.6:c.5503-123_5503-117delinsTTCTCCA MANE Select	NP_071407.4:n.5503-123_5503-117delinsTTCTCCA