Canonical Allele Identifier: CA2843744664

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740904del , CM000672.2:g.71740904del	GRCh38
NC_000010.10:g.73500661del , CM000672.1:g.73500661del	GRCh37
NC_000010.9:g.73170667del	NCBI36
NG_008835.1:g.348958del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4571del MANE Select	ENSP00000224721.9:p.Pro1524LeufsTer14
ENST00000224721.10:c.4586del	ENSP00000224721.8:p.Pro1529LeufsTer14
ENST00000398792.3:n.1260del
ENST00000622827.4:c.4571del	ENSP00000483211.1:p.Pro1524LeufsTer14
NM_022124.5:c.4571del	NP_071407.4:p.Pro1524LeufsTer14
XM_006717940.2:c.4766del	XP_006718003.1:p.Pro1589LeufsTer14
XM_006717942.2:c.4700del	XP_006718005.1:p.Pro1567LeufsTer14
XM_011540039.1:c.4763del	XP_011538341.1:p.Pro1588LeufsTer14
XM_011540040.1:c.4760del	XP_011538342.1:p.Pro1587LeufsTer14
XM_011540041.1:c.4706del	XP_011538343.1:p.Pro1569LeufsTer14
XM_011540042.1:c.4766del	XP_011538344.1:p.Pro1589LeufsTer14
XM_011540043.1:c.4766del	XP_011538345.1:p.Pro1589LeufsTer14
XM_011540044.1:c.4631del	XP_011538346.1:p.Pro1544LeufsTer14
XM_011540045.1:c.4766del	XP_011538347.1:p.Pro1589LeufsTer14
XM_011540046.1:c.4226del	XP_011538348.1:p.Pro1409LeufsTer14
XM_011540047.1:c.3584del	XP_011538349.1:p.Pro1195LeufsTer14
XM_011540048.1:c.4766del	XP_011538350.1:p.Pro1589LeufsTer14
XM_011540049.1:c.4766del	XP_011538351.1:p.Pro1589LeufsTer14
XM_011540050.1:c.4766del	XP_011538352.1:p.Pro1589LeufsTer14
XM_011540051.1:c.4766del	XP_011538353.1:p.Pro1589LeufsTer14
XM_011540052.1:c.1094del	XP_011538354.1:p.Pro365LeufsTer14
XM_011540053.1:c.4766del	XP_011538355.1:p.Pro1589LeufsTer14
XR_945796.1:n.5009del
NM_022124.6:c.4571del MANE Select	NP_071407.4:p.Pro1524LeufsTer14