Canonical Allele Identifier: CA2788480883

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785118_71785119insAGAT , CM000672.2:g.71785118_71785119insAGAT	GRCh38
NC_000010.10:g.73544875_73544876insAGAT , CM000672.1:g.73544875_73544876insAGAT	GRCh37
NC_000010.9:g.73214881_73214882insAGAT	NCBI36
NG_008835.1:g.393172_393173insAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5712+18_5712+19insAGAT MANE Select	ENSP00000224721.9:n.5712+18_5712+19insAGAT
ENST00000224721.10:c.5727+18_5727+19insAGAT	ENSP00000224721.8:n.5727+18_5727+19insAGAT
ENST00000622827.4:c.5712+18_5712+19insAGAT	ENSP00000483211.1:n.5712+18_5712+19insAGAT
NM_022124.5:c.5712+18_5712+19insAGAT	NP_071407.4:n.5712+18_5712+19insAGAT
XM_006717940.2:c.5907+18_5907+19insAGAT	XP_006718003.1:n.5907+18_5907+19insAGAT
XM_006717942.2:c.5841+18_5841+19insAGAT	XP_006718005.1:n.5841+18_5841+19insAGAT
XM_011540039.1:c.5904+18_5904+19insAGAT	XP_011538341.1:n.5904+18_5904+19insAGAT
XM_011540040.1:c.5901+18_5901+19insAGAT	XP_011538342.1:n.5901+18_5901+19insAGAT
XM_011540041.1:c.5847+18_5847+19insAGAT	XP_011538343.1:n.5847+18_5847+19insAGAT
XM_011540042.1:c.5907+18_5907+19insAGAT	XP_011538344.1:n.5907+18_5907+19insAGAT
XM_011540043.1:c.5907+18_5907+19insAGAT	XP_011538345.1:n.5907+18_5907+19insAGAT
XM_011540044.1:c.5772+18_5772+19insAGAT	XP_011538346.1:n.5772+18_5772+19insAGAT
XM_011540045.1:c.5907+18_5907+19insAGAT	XP_011538347.1:n.5907+18_5907+19insAGAT
XM_011540046.1:c.5367+18_5367+19insAGAT	XP_011538348.1:n.5367+18_5367+19insAGAT
XM_011540047.1:c.4725+18_4725+19insAGAT	XP_011538349.1:n.4725+18_4725+19insAGAT
XM_011540048.1:c.5907+18_5907+19insAGAT	XP_011538350.1:n.5907+18_5907+19insAGAT
XM_011540049.1:c.5907+18_5907+19insAGAT	XP_011538351.1:n.5907+18_5907+19insAGAT
XM_011540050.1:c.5907+18_5907+19insAGAT	XP_011538352.1:n.5907+18_5907+19insAGAT
XM_011540051.1:c.5907+18_5907+19insAGAT	XP_011538353.1:n.5907+18_5907+19insAGAT
XM_011540052.1:c.2235+18_2235+19insAGAT	XP_011538354.1:n.2235+18_2235+19insAGAT
XM_011540053.1:c.5907+18_5907+19insAGAT	XP_011538355.1:n.5907+18_5907+19insAGAT
XR_945796.1:n.6150+18_6150+19insAGAT
NM_022124.6:c.5712+18_5712+19insAGAT MANE Select	NP_071407.4:n.5712+18_5712+19insAGAT