Canonical Allele Identifier: CA2842194573
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29673263dup , CM000684.2:g.29673263dup GRCh38
NC_000022.10:g.30069252dup , CM000684.1:g.30069252dup GRCh37
NC_000022.9:g.28399252dup NCBI36
NG_009057.1:g.74708dup , LRG_511:g.74708dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000361166.10:c.988-6dup ENSP00000354529.6:n.988-6dup
ENST00000673312.2:c.*617-6dup ENSP00000500186.2:n.*617-6dup
ENST00000338641.10:c.1123-6dup MANE Select ENSP00000344666.5:n.1123-6dup
ENST00000361166.9:c.541-6dup ENSP00000354529.5:n.541-6dup
ENST00000672461.1:c.1123-6dup ENSP00000500919.1:n.1123-6dup
ENST00000672805.1:c.*1005-6dup ENSP00000500295.1:n.*1005-6dup
ENST00000672896.1:c.1123-6dup ENSP00000500117.1:n.1123-6dup
ENST00000673312.1:c.1142-6dup ENSP00000500186.1:n.1142-6dup
ENST00000334961.11:c.874-6dup ENSP00000335652.7:n.874-6dup
ENST00000338641.8:c.1123-6dup ENSP00000344666.4:n.1123-6dup
ENST00000353887.8:c.874-6dup ENSP00000340626.4:n.874-6dup
ENST00000361166.8:c.1123-6dup ENSP00000354529.4:n.1123-6dup
ENST00000361452.8:c.1000-6dup ENSP00000354897.4:n.1000-6dup
ENST00000361676.8:c.997-6dup ENSP00000355183.4:n.997-6dup
ENST00000397789.3:c.1123-6dup ENSP00000380891.3:n.1123-6dup
ENST00000403435.5:c.1036-6dup ENSP00000384029.1:n.1036-6dup
ENST00000403999.7:c.1123-6dup ENSP00000384797.3:n.1123-6dup
ENST00000413209.6:c.448-21489dup ENSP00000409921.2:n.448-21489dup
ENST00000432151.5:c.523-1573dup ENSP00000395885.1:n.523-1573dup
NM_000268.3:c.1123-6dup , LRG_511t1:c.1123-6dup NP_000259.1:n.1123-6dup
NM_016418.5:c.1123-6dup , LRG_511t2:c.1123-6dup NP_057502.2:n.1123-6dup
NM_181825.2:c.1123-6dup NP_861546.1:n.1123-6dup
NM_181828.2:c.997-6dup NP_861966.1:n.997-6dup
NM_181829.2:c.1000-6dup NP_861967.1:n.1000-6dup
NM_181830.2:c.874-6dup NP_861968.1:n.874-6dup
NM_181831.2:c.874-6dup NP_861969.1:n.874-6dup
NM_181832.2:c.1123-6dup NP_861970.1:n.1123-6dup
NM_181833.2:c.448-21489dup NP_861971.1:n.448-21489dup
NR_156186.1:n.1682-6dup
XM_017028809.2:c.1009-6dup XP_016884298.1:n.1009-6dup
XM_017028810.1:c.1009-6dup XP_016884299.1:n.1009-6dup
NM_000268.4:c.1123-6dup MANE Select NP_000259.1:n.1123-6dup
NM_181825.3:c.1123-6dup NP_861546.1:n.1123-6dup
NM_181828.3:c.997-6dup NP_861966.1:n.997-6dup
NM_181829.3:c.1000-6dup NP_861967.1:n.1000-6dup
NM_181830.3:c.874-6dup NP_861968.1:n.874-6dup
NM_181831.3:c.874-6dup NP_861969.1:n.874-6dup
NM_181832.3:c.1123-6dup NP_861970.1:n.1123-6dup
NR_156186.2:n.1605-6dup
NM_181833.3:c.448-21489dup NP_861971.1:n.448-21489dup