Canonical Allele Identifier: CA2788483490
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71812665del , CM000672.2:g.71812665del GRCh38
NC_000010.10:g.73572422del , CM000672.1:g.73572422del GRCh37
NC_000010.9:g.73242428del NCBI36
NG_008835.1:g.420719del

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.9510+56del MANE Select ENSP00000224721.9:n.9510+56del
ENST00000642965.1:c.3443+56del ENSP00000495222.1:n.3443+56del
ENST00000647092.1:c.3107+56del ENSP00000495176.1:n.3107+56del
ENST00000224721.10:c.9525+56del ENSP00000224721.8:n.9525+56del
ENST00000398788.4:c.2790+56del ENSP00000381768.3:n.2790+56del
ENST00000475158.1:n.3046+56del
ENST00000619887.4:c.2790+56del ENSP00000478374.1:n.2790+56del
ENST00000622827.4:c.9510+56del ENSP00000483211.1:n.9510+56del
NM_001171933.1:c.2790+56del NP_001165404.1:n.2790+56del
NM_001171934.1:c.2790+56del NP_001165405.1:n.2790+56del
NM_001171935.1:c.201+56del NP_001165406.1:n.201+56del
NM_001171936.1:c.201+56del NP_001165407.1:n.201+56del
NM_022124.5:c.9510+56del NP_071407.4:n.9510+56del
XM_006717940.2:c.9705+56del XP_006718003.1:n.9705+56del
XM_006717942.2:c.9639+56del XP_006718005.1:n.9639+56del
XM_011540039.1:c.9702+56del XP_011538341.1:n.9702+56del
XM_011540040.1:c.9699+56del XP_011538342.1:n.9699+56del
XM_011540041.1:c.9645+56del XP_011538343.1:n.9645+56del
XM_011540042.1:c.9615+56del XP_011538344.1:n.9615+56del
XM_011540043.1:c.9705+56del XP_011538345.1:n.9705+56del
XM_011540044.1:c.9570+56del XP_011538346.1:n.9570+56del
XM_011540045.1:c.9705+56del XP_011538347.1:n.9705+56del
XM_011540046.1:c.9165+56del XP_011538348.1:n.9165+56del
XM_011540047.1:c.8523+56del XP_011538349.1:n.8523+56del
XM_011540052.1:c.6033+56del XP_011538354.1:n.6033+56del
NM_022124.6:c.9510+56del MANE Select NP_071407.4:n.9510+56del