Canonical Allele Identifier: CA2656032158
Gene: NF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29674869del , CM000684.2:g.29674869del GRCh38
NC_000022.10:g.30070858del , CM000684.1:g.30070858del GRCh37
NC_000022.9:g.28400858del NCBI36
NG_009057.1:g.76314del , LRG_511:g.76314del

Transcript Alleles

HGVS Amino-acid change
ENST00000361166.10:c.1239del ENSP00000354529.6:p.Gln414ArgfsTer26
ENST00000673312.2:c.*868del ENSP00000500186.2:n.*868del
ENST00000338641.10:c.1374del MANE Select ENSP00000344666.5:p.Gln459ArgfsTer26
ENST00000361166.9:c.792del ENSP00000354529.5:p.Gln265ArgfsTer26
ENST00000672461.1:c.1374del ENSP00000500919.1:p.Gln459ArgfsTer26
ENST00000672805.1:c.*1256del ENSP00000500295.1:n.*1256del
ENST00000672896.1:c.1374del ENSP00000500117.1:p.Gln459ArgfsTer26
ENST00000673312.1:c.1393del ENSP00000500186.1:n.1393del
ENST00000334961.11:c.1125del ENSP00000335652.7:p.Gln376ArgfsTer26
ENST00000338641.8:c.1374del ENSP00000344666.4:p.Gln459ArgfsTer26
ENST00000353887.8:c.1125del ENSP00000340626.4:p.Gln376ArgfsTer26
ENST00000361166.8:c.1374del ENSP00000354529.4:p.Gln459ArgfsTer26
ENST00000361452.8:c.1251del ENSP00000354897.4:p.Gln418ArgfsTer26
ENST00000361676.8:c.1248del ENSP00000355183.4:p.Gln417ArgfsTer26
ENST00000397789.3:c.1374del ENSP00000380891.3:p.Gln459ArgfsTer26
ENST00000403435.5:c.1287del ENSP00000384029.1:p.Gln430ArgfsTer26
ENST00000403999.7:c.1374del ENSP00000384797.3:p.Gln459ArgfsTer26
ENST00000413209.6:c.448-19883del ENSP00000409921.2:n.448-19883del
ENST00000432151.5:c.556del ENSP00000395885.1:p.Ala186GlnfsTer?
NM_000268.3:c.1374del , LRG_511t1:c.1374del NP_000259.1:p.Gln459ArgfsTer26
NM_016418.5:c.1374del , LRG_511t2:c.1374del NP_057502.2:p.Gln459ArgfsTer26
NM_181825.2:c.1374del NP_861546.1:p.Gln459ArgfsTer26
NM_181828.2:c.1248del NP_861966.1:p.Gln417ArgfsTer26
NM_181829.2:c.1251del NP_861967.1:p.Gln418ArgfsTer26
NM_181830.2:c.1125del NP_861968.1:p.Gln376ArgfsTer26
NM_181831.2:c.1125del NP_861969.1:p.Gln376ArgfsTer26
NM_181832.2:c.1374del NP_861970.1:p.Gln459ArgfsTer26
NM_181833.2:c.448-19883del NP_861971.1:n.448-19883del
NR_156186.1:n.1933del
XM_017028809.2:c.1260del XP_016884298.1:p.Gln421ArgfsTer26
XM_017028810.1:c.1260del XP_016884299.1:p.Gln421ArgfsTer26
NM_000268.4:c.1374del MANE Select NP_000259.1:p.Gln459ArgfsTer26
NM_181825.3:c.1374del NP_861546.1:p.Gln459ArgfsTer26
NM_181828.3:c.1248del NP_861966.1:p.Gln417ArgfsTer26
NM_181829.3:c.1251del NP_861967.1:p.Gln418ArgfsTer26
NM_181830.3:c.1125del NP_861968.1:p.Gln376ArgfsTer26
NM_181831.3:c.1125del NP_861969.1:p.Gln376ArgfsTer26
NM_181832.3:c.1374del NP_861970.1:p.Gln459ArgfsTer26
NR_156186.2:n.1856del
NM_181833.3:c.448-19883del NP_861971.1:n.448-19883del