Canonical Allele Identifier: CA1918878956
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71799637_71799649delinsGTGATGGAGGGCC , CM000672.2:g.71799637_71799649delinsGTGATGGAGGGCC GRCh38
NC_000010.10:g.73559394_73559406delinsGTGATGGAGGGCC , CM000672.1:g.73559394_73559406delinsGTGATGGAGGGCC GRCh37
NC_000010.9:g.73229400_73229412delinsGTGATGGAGGGCC NCBI36
NG_008835.1:g.407691_407703delinsGTGATGGAGGGCC

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.7362+8_7362+20delinsGTGATGGAGGGCC MANE Select ENSP00000224721.9:n.7362+8_7362+20delinsG...
ENST00000642965.1:c.1295+8_1295+20delinsGTGATGGAGGGCC ENSP00000495222.1:n.1295+8_1295+20delinsG...
ENST00000647092.1:c.959+8_959+20delinsGTGATGGAGGGCC ENSP00000495176.1:n.959+8_959+20delinsGTG...
ENST00000224721.10:c.7377+8_7377+20delinsGTGATGGAGGGCC ENSP00000224721.8:n.7377+8_7377+20delinsG...
ENST00000398788.4:c.642+8_642+20delinsGTGATGGAGGGCC ENSP00000381768.3:n.642+8_642+20delinsGTG...
ENST00000475158.1:n.898+8_898+20delinsGTGATGGAGGGCC
ENST00000619887.4:c.642+8_642+20delinsGTGATGGAGGGCC ENSP00000478374.1:n.642+8_642+20delinsGTG...
ENST00000622827.4:c.7362+8_7362+20delinsGTGATGGAGGGCC ENSP00000483211.1:n.7362+8_7362+20delinsG...
NM_001171933.1:c.642+8_642+20delinsGTGATGGAGGGCC NP_001165404.1:n.642+8_642+20delinsGTGATG...
NM_001171934.1:c.642+8_642+20delinsGTGATGGAGGGCC NP_001165405.1:n.642+8_642+20delinsGTGATG...
NM_022124.5:c.7362+8_7362+20delinsGTGATGGAGGGCC NP_071407.4:n.7362+8_7362+20delinsGTGATGG...
XM_006717940.2:c.7557+8_7557+20delinsGTGATGGAGGGCC XP_006718003.1:n.7557+8_7557+20delinsGTGA...
XM_006717942.2:c.7491+8_7491+20delinsGTGATGGAGGGCC XP_006718005.1:n.7491+8_7491+20delinsGTGA...
XM_011540039.1:c.7554+8_7554+20delinsGTGATGGAGGGCC XP_011538341.1:n.7554+8_7554+20delinsGTGA...
XM_011540040.1:c.7551+8_7551+20delinsGTGATGGAGGGCC XP_011538342.1:n.7551+8_7551+20delinsGTGA...
XM_011540041.1:c.7497+8_7497+20delinsGTGATGGAGGGCC XP_011538343.1:n.7497+8_7497+20delinsGTGA...
XM_011540042.1:c.7467+8_7467+20delinsGTGATGGAGGGCC XP_011538344.1:n.7467+8_7467+20delinsGTGA...
XM_011540043.1:c.7557+8_7557+20delinsGTGATGGAGGGCC XP_011538345.1:n.7557+8_7557+20delinsGTGA...
XM_011540044.1:c.7422+8_7422+20delinsGTGATGGAGGGCC XP_011538346.1:n.7422+8_7422+20delinsGTGA...
XM_011540045.1:c.7557+8_7557+20delinsGTGATGGAGGGCC XP_011538347.1:n.7557+8_7557+20delinsGTGA...
XM_011540046.1:c.7017+8_7017+20delinsGTGATGGAGGGCC XP_011538348.1:n.7017+8_7017+20delinsGTGA...
XM_011540047.1:c.6375+8_6375+20delinsGTGATGGAGGGCC XP_011538349.1:n.6375+8_6375+20delinsGTGA...
XM_011540052.1:c.3885+8_3885+20delinsGTGATGGAGGGCC XP_011538354.1:n.3885+8_3885+20delinsGTGA...
NM_022124.6:c.7362+8_7362+20delinsGTGATGGAGGGCC MANE Select NP_071407.4:n.7362+8_7362+20delinsGTGATGG...