Canonical Allele Identifier: CA2818684351
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29674761del , CM000684.2:g.29674761del GRCh38
NC_000022.10:g.30070750del , CM000684.1:g.30070750del GRCh37
NC_000022.9:g.28400750del NCBI36
NG_009057.1:g.76206del , LRG_511:g.76206del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361166.10:c.1206-75del ENSP00000354529.6:n.1206-75del
ENST00000673312.2:c.*835-75del ENSP00000500186.2:n.*835-75del
ENST00000338641.10:c.1341-75del MANE Select ENSP00000344666.5:n.1341-75del
ENST00000361166.9:c.759-75del ENSP00000354529.5:n.759-75del
ENST00000672461.1:c.1341-75del ENSP00000500919.1:n.1341-75del
ENST00000672805.1:c.*1223-75del ENSP00000500295.1:n.*1223-75del
ENST00000672896.1:c.1341-75del ENSP00000500117.1:n.1341-75del
ENST00000673312.1:c.1360-75del ENSP00000500186.1:n.1360-75del
ENST00000334961.11:c.1092-75del ENSP00000335652.7:n.1092-75del
ENST00000338641.8:c.1341-75del ENSP00000344666.4:n.1341-75del
ENST00000353887.8:c.1092-75del ENSP00000340626.4:n.1092-75del
ENST00000361166.8:c.1341-75del ENSP00000354529.4:n.1341-75del
ENST00000361452.8:c.1218-75del ENSP00000354897.4:n.1218-75del
ENST00000361676.8:c.1215-75del ENSP00000355183.4:n.1215-75del
ENST00000397789.3:c.1341-75del ENSP00000380891.3:n.1341-75del
ENST00000403435.5:c.1254-75del ENSP00000384029.1:n.1254-75del
ENST00000403999.7:c.1341-75del ENSP00000384797.3:n.1341-75del
ENST00000413209.6:c.448-19991del ENSP00000409921.2:n.448-19991del
ENST00000432151.5:c.523-75del ENSP00000395885.1:n.523-75del
NM_000268.3:c.1341-75del , LRG_511t1:c.1341-75del NP_000259.1:n.1341-75del
NM_016418.5:c.1341-75del , LRG_511t2:c.1341-75del NP_057502.2:n.1341-75del
NM_181825.2:c.1341-75del NP_861546.1:n.1341-75del
NM_181828.2:c.1215-75del NP_861966.1:n.1215-75del
NM_181829.2:c.1218-75del NP_861967.1:n.1218-75del
NM_181830.2:c.1092-75del NP_861968.1:n.1092-75del
NM_181831.2:c.1092-75del NP_861969.1:n.1092-75del
NM_181832.2:c.1341-75del NP_861970.1:n.1341-75del
NM_181833.2:c.448-19991del NP_861971.1:n.448-19991del
NR_156186.1:n.1900-75del
XM_017028809.2:c.1227-75del XP_016884298.1:n.1227-75del
XM_017028810.1:c.1227-75del XP_016884299.1:n.1227-75del
NM_000268.4:c.1341-75del MANE Select NP_000259.1:n.1341-75del
NM_181825.3:c.1341-75del NP_861546.1:n.1341-75del
NM_181828.3:c.1215-75del NP_861966.1:n.1215-75del
NM_181829.3:c.1218-75del NP_861967.1:n.1218-75del
NM_181830.3:c.1092-75del NP_861968.1:n.1092-75del
NM_181831.3:c.1092-75del NP_861969.1:n.1092-75del
NM_181832.3:c.1341-75del NP_861970.1:n.1341-75del
NR_156186.2:n.1823-75del
NM_181833.3:c.448-19991del NP_861971.1:n.448-19991del