Canonical Allele Identifier: CA2400692922
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29696093_29696118delinsAGATGGAGTCTCTCTCTGTCACCCAG , CM000684.2:g.29696093_29696118delinsAGATGGAGTCTCTCTCTGTCACCCAG GRCh38
NC_000022.10:g.30092082_30092107delinsAGATGGAGTCTCTCTCTGTCACCCAG , CM000684.1:g.30092082_30092107delinsAGATGGAGTCTCTCTCTGTCACCCAG GRCh37
NC_000022.9:g.28422082_28422107delinsAGATGGAGTCTCTCTCTGTCACCCAG NCBI36
NG_009057.1:g.97538_97563delinsAGATGGAGTCTCTCTCTGTCACCCAG , LRG_511:g.97538_97563delinsAGATGGAGTCTCTCTCTGTCACCCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000338641.10:c.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCCAG MANE Select ENSP00000344666.5:n.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCC...
ENST00000672461.1:c.*501+850_*501+875delinsAGATGGAGTCTCTCTCTGTCACCCAG ENSP00000500919.1:n.*501+850_*501+875delinsAGATGGAGTCTCTCTCTG...
ENST00000672896.1:c.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG ENSP00000500117.1:n.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCC...
ENST00000338641.8:c.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCCAG ENSP00000344666.4:n.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCC...
ENST00000361452.8:c.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG ENSP00000354897.4:n.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCC...
ENST00000413209.6:c.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCCAG ENSP00000409921.2:n.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCC...
NM_000268.3:c.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCCAG , LRG_511t1:c.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCCAG NP_000259.1:n.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCCAG
NM_016418.5:c.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG , LRG_511t2:c.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG NP_057502.2:n.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG
NM_181828.2:c.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG NP_861966.1:n.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG
NM_181829.2:c.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG NP_861967.1:n.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG
NM_181830.2:c.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG NP_861968.1:n.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG
NM_181832.2:c.*1366_*1391delinsAGATGGAGTCTCTCTCTGTCACCCAG NP_861970.1:n.*1366_*1391delinsAGATGGAGTCTCTCTCTGTCACCCAG
NM_181833.2:c.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCCAG NP_861971.1:n.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCCAG
NR_156186.1:n.3638_3663delinsAGATGGAGTCTCTCTCTGTCACCCAG
XM_017028810.1:c.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG XP_016884299.1:n.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG
NM_000268.4:c.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCCAG MANE Select NP_000259.1:n.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCCAG
NM_181828.3:c.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG NP_861966.1:n.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG
NM_181829.3:c.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG NP_861967.1:n.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG
NM_181830.3:c.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG NP_861968.1:n.*1351_*1376delinsAGATGGAGTCTCTCTCTGTCACCCAG
NM_181832.3:c.*1366_*1391delinsAGATGGAGTCTCTCTCTGTCACCCAG NP_861970.1:n.*1366_*1391delinsAGATGGAGTCTCTCTCTGTCACCCAG
NR_156186.2:n.3561_3586delinsAGATGGAGTCTCTCTCTGTCACCCAG
NM_181833.3:c.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCCAG NP_861971.1:n.*1291_*1316delinsAGATGGAGTCTCTCTCTGTCACCCAG