Canonical Allele Identifier: CA2516649282
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29696077_29696078insA , CM000684.2:g.29696077_29696078insA GRCh38
NC_000022.10:g.30092066_30092067insA , CM000684.1:g.30092066_30092067insA GRCh37
NC_000022.9:g.28422066_28422067insA NCBI36
NG_009057.1:g.97522_97523insA , LRG_511:g.97522_97523insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000338641.10:c.*1275_*1276insA MANE Select ENSP00000344666.5:n.*1275_*1276insA
ENST00000672461.1:c.*501+834_*501+835insA ENSP00000500919.1:n.*501+834_*501+835insA
ENST00000672896.1:c.*1335_*1336insA ENSP00000500117.1:n.*1335_*1336insA
ENST00000338641.8:c.*1275_*1276insA ENSP00000344666.4:n.*1275_*1276insA
ENST00000361452.8:c.*1335_*1336insA ENSP00000354897.4:n.*1335_*1336insA
ENST00000413209.6:c.*1275_*1276insA ENSP00000409921.2:n.*1275_*1276insA
NM_000268.3:c.*1275_*1276insA , LRG_511t1:c.*1275_*1276insA NP_000259.1:n.*1275_*1276insA
NM_016418.5:c.*1335_*1336insA , LRG_511t2:c.*1335_*1336insA NP_057502.2:n.*1335_*1336insA
NM_181828.2:c.*1335_*1336insA NP_861966.1:n.*1335_*1336insA
NM_181829.2:c.*1335_*1336insA NP_861967.1:n.*1335_*1336insA
NM_181830.2:c.*1335_*1336insA NP_861968.1:n.*1335_*1336insA
NM_181832.2:c.*1350_*1351insA NP_861970.1:n.*1350_*1351insA
NM_181833.2:c.*1275_*1276insA NP_861971.1:n.*1275_*1276insA
NR_156186.1:n.3622_3623insA
XM_017028810.1:c.*1335_*1336insA XP_016884299.1:n.*1335_*1336insA
NM_000268.4:c.*1275_*1276insA MANE Select NP_000259.1:n.*1275_*1276insA
NM_181828.3:c.*1335_*1336insA NP_861966.1:n.*1335_*1336insA
NM_181829.3:c.*1335_*1336insA NP_861967.1:n.*1335_*1336insA
NM_181830.3:c.*1335_*1336insA NP_861968.1:n.*1335_*1336insA
NM_181832.3:c.*1350_*1351insA NP_861970.1:n.*1350_*1351insA
NR_156186.2:n.3545_3546insA
NM_181833.3:c.*1275_*1276insA NP_861971.1:n.*1275_*1276insA