Canonical Allele Identifier: CA1024927463
Gene: NF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29696089_29696090insTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000684.2:g.29696089_29696090insTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000022.10:g.30092078_30092079insTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000684.1:g.30092078_30092079insTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000022.9:g.28422078_28422079insTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_009057.1:g.97534_97535insTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_511:g.97534_97535insTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000338641.10:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000344666.5:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000672461.1:c.*501+846_*501+847insTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000500919.1:n.*501+846_*501+847insTTTTTTTTTTTTTTTTTTTTT...
ENST00000672896.1:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000500117.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000338641.8:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000344666.4:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000361452.8:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000354897.4:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000413209.6:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000409921.2:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_000268.3:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_511t1:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_000259.1:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_016418.5:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_511t2:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_057502.2:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181828.2:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_861966.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181829.2:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_861967.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181830.2:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_861968.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181832.2:c.*1362_*1363insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_861970.1:n.*1362_*1363insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181833.2:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_861971.1:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT
NR_156186.1:n.3634_3635insTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_017028810.1:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016884299.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_000268.4:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_000259.1:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181828.3:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_861966.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181829.3:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_861967.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181830.3:c.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_861968.1:n.*1347_*1348insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181832.3:c.*1362_*1363insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_861970.1:n.*1362_*1363insTTTTTTTTTTTTTTTTTTTTTTTTTT
NR_156186.2:n.3557_3558insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_181833.3:c.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_861971.1:n.*1287_*1288insTTTTTTTTTTTTTTTTTTTTTTTTTT