Canonical Allele Identifier: CA5543259

Gene: CDH23

Linked Data

• dbSNP Id: rs760684736
• ExAC: 10:73199558 CCTCTT / C
• gnomAD v2: 10-73199558-CCTCTT-C
• gnomAD v4: 10-71439801-CCTCTT-C
• MyVariant Identifiers: chr10:g.73199559_73199563del (hg19) ; chr10:g.71439802_71439806del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71439807_71439811del , CM000672.2:g.71439807_71439811del	GRCh38
NC_000010.10:g.73199564_73199568del , CM000672.1:g.73199564_73199568del	GRCh37
NC_000010.9:g.72869570_72869574del	NCBI36
NG_008835.1:g.47861_47865del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.-5-20_-5-16del MANE Select	ENSP00000224721.9:n.-5-20_-5-16del
ENST00000398809.9:c.-5-20_-5-16del	ENSP00000381789.5:n.-5-20_-5-16del
ENST00000644511.1:c.130+42489_130+42493del	ENSP00000495691.1:n.130+42489_130+42493del
ENST00000224721.10:c.-5-20_-5-16del	ENSP00000224721.8:n.-5-20_-5-16del
ENST00000299366.11:c.-5-20_-5-16del	ENSP00000299366.8:n.-5-20_-5-16del
ENST00000398809.8:c.-5-20_-5-16del	ENSP00000381789.5:n.-5-20_-5-16del
ENST00000398842.7:c.-33+42489_-33+42493del	ENSP00000381822.4:n.-33+42489_-33+42493del
ENST00000461841.7:c.-5-20_-5-16del	ENSP00000473454.2:n.-5-20_-5-16del
ENST00000616684.4:c.-5-20_-5-16del	ENSP00000482036.2:n.-5-20_-5-16del
ENST00000622827.4:c.-5-20_-5-16del	ENSP00000483211.1:n.-5-20_-5-16del
NM_001171930.1:c.-5-20_-5-16del	NP_001165401.1:n.-5-20_-5-16del
NM_001171931.1:c.-5-20_-5-16del	NP_001165402.1:n.-5-20_-5-16del
NM_001171932.1:c.-5-20_-5-16del	NP_001165403.1:n.-5-20_-5-16del
NM_022124.5:c.-5-20_-5-16del	NP_071407.4:n.-5-20_-5-16del
NM_052836.3:c.-5-20_-5-16del	NP_443068.1:n.-5-20_-5-16del
XM_006717940.2:c.131-20_131-16del	XP_006718003.1:n.131-20_131-16del
XM_006717942.2:c.131-20_131-16del	XP_006718005.1:n.131-20_131-16del
XM_011540039.1:c.131-20_131-16del	XP_011538341.1:n.131-20_131-16del
XM_011540040.1:c.131-20_131-16del	XP_011538342.1:n.131-20_131-16del
XM_011540041.1:c.131-20_131-16del	XP_011538343.1:n.131-20_131-16del
XM_011540042.1:c.131-20_131-16del	XP_011538344.1:n.131-20_131-16del
XM_011540043.1:c.131-20_131-16del	XP_011538345.1:n.131-20_131-16del
XM_011540044.1:c.-5-20_-5-16del	XP_011538346.1:n.-5-20_-5-16del
XM_011540045.1:c.131-20_131-16del	XP_011538347.1:n.131-20_131-16del
XM_011540048.1:c.131-20_131-16del	XP_011538350.1:n.131-20_131-16del
XM_011540049.1:c.131-20_131-16del	XP_011538351.1:n.131-20_131-16del
XM_011540050.1:c.131-20_131-16del	XP_011538352.1:n.131-20_131-16del
XM_011540051.1:c.131-20_131-16del	XP_011538353.1:n.131-20_131-16del
XM_011540053.1:c.131-20_131-16del	XP_011538355.1:n.131-20_131-16del
XM_011540054.1:c.131-20_131-16del	XP_011538356.1:n.131-20_131-16del
XR_945796.1:n.374-20_374-16del
NM_001171930.2:c.-5-20_-5-16del	NP_001165401.1:n.-5-20_-5-16del
NM_001171931.2:c.-5-20_-5-16del	NP_001165402.1:n.-5-20_-5-16del
NM_022124.6:c.-5-20_-5-16del MANE Select	NP_071407.4:n.-5-20_-5-16del
NM_052836.4:c.-5-20_-5-16del	NP_443068.1:n.-5-20_-5-16del
NM_001171932.2:c.-5-20_-5-16del	NP_001165403.1:n.-5-20_-5-16del