Canonical Allele Identifier: CA1024927508
Gene: NF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29696089_29696090insTTTTTTTTTTTTTTTTTTTTTTTTT , CM000684.2:g.29696089_29696090insTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000022.10:g.30092078_30092079insTTTTTTTTTTTTTTTTTTTTTTTTT , CM000684.1:g.30092078_30092079insTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000022.9:g.28422078_28422079insTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_009057.1:g.97534_97535insTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_511:g.97534_97535insTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000338641.10:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000344666.5:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000672461.1:c.*501+846_*501+847insTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000500919.1:n.*501+846_*501+847insTTTTTTTTTTTTTTTTTTTTT...
ENST00000672896.1:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000500117.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000338641.8:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000344666.4:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000361452.8:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000354897.4:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000413209.6:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000409921.2:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_000268.3:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_511t1:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT NP_000259.1:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_016418.5:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_511t2:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT NP_057502.2:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181828.2:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT NP_861966.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181829.2:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT NP_861967.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181830.2:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT NP_861968.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181832.2:c.*1362_*1363insTTTTTTTTTTTTTTTTTTTTTTTTT NP_861970.1:n.*1362_*1363insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181833.2:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT NP_861971.1:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT
NR_156186.1:n.3634_3635insTTTTTTTTTTTTTTTTTTTTTTTTT
XM_017028810.1:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT XP_016884299.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_000268.4:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_000259.1:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181828.3:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT NP_861966.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181829.3:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT NP_861967.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181830.3:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT NP_861968.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181832.3:c.*1362_*1363insTTTTTTTTTTTTTTTTTTTTTTTTT NP_861970.1:n.*1362_*1363insTTTTTTTTTTTTTTTTTTTTTTTTT
NR_156186.2:n.3557_3558insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181833.3:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT NP_861971.1:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTT