Canonical Allele Identifier: CA2577681299
Gene: NF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29673194_29673195insG , CM000684.2:g.29673194_29673195insG GRCh38
NC_000022.10:g.30069183_30069184insG , CM000684.1:g.30069183_30069184insG GRCh37
NC_000022.9:g.28399183_28399184insG NCBI36
NG_009057.1:g.74639_74640insG , LRG_511:g.74639_74640insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000361166.10:c.988-75_988-74insG ENSP00000354529.6:n.988-75_988-74insG
ENST00000673312.2:c.*617-75_*617-74insG ENSP00000500186.2:n.*617-75_*617-74insG
ENST00000338641.10:c.1123-75_1123-74insG MANE Select ENSP00000344666.5:n.1123-75_1123-74insG
ENST00000361166.9:c.541-75_541-74insG ENSP00000354529.5:n.541-75_541-74insG
ENST00000672461.1:c.1123-75_1123-74insG ENSP00000500919.1:n.1123-75_1123-74insG
ENST00000672805.1:c.*1005-75_*1005-74insG ENSP00000500295.1:n.*1005-75_*1005-74insG
ENST00000672896.1:c.1123-75_1123-74insG ENSP00000500117.1:n.1123-75_1123-74insG
ENST00000673312.1:c.1142-75_1142-74insG ENSP00000500186.1:n.1142-75_1142-74insG
ENST00000334961.11:c.874-75_874-74insG ENSP00000335652.7:n.874-75_874-74insG
ENST00000338641.8:c.1123-75_1123-74insG ENSP00000344666.4:n.1123-75_1123-74insG
ENST00000353887.8:c.874-75_874-74insG ENSP00000340626.4:n.874-75_874-74insG
ENST00000361166.8:c.1123-75_1123-74insG ENSP00000354529.4:n.1123-75_1123-74insG
ENST00000361452.8:c.1000-75_1000-74insG ENSP00000354897.4:n.1000-75_1000-74insG
ENST00000361676.8:c.997-75_997-74insG ENSP00000355183.4:n.997-75_997-74insG
ENST00000397789.3:c.1123-75_1123-74insG ENSP00000380891.3:n.1123-75_1123-74insG
ENST00000403435.5:c.1036-75_1036-74insG ENSP00000384029.1:n.1036-75_1036-74insG
ENST00000403999.7:c.1123-75_1123-74insG ENSP00000384797.3:n.1123-75_1123-74insG
ENST00000413209.6:c.448-21558_448-21557insG ENSP00000409921.2:n.448-21558_448-21557insG
ENST00000432151.5:c.523-1642_523-1641insG ENSP00000395885.1:n.523-1642_523-1641insG
NM_000268.3:c.1123-75_1123-74insG , LRG_511t1:c.1123-75_1123-74insG NP_000259.1:n.1123-75_1123-74insG
NM_016418.5:c.1123-75_1123-74insG , LRG_511t2:c.1123-75_1123-74insG NP_057502.2:n.1123-75_1123-74insG
NM_181825.2:c.1123-75_1123-74insG NP_861546.1:n.1123-75_1123-74insG
NM_181828.2:c.997-75_997-74insG NP_861966.1:n.997-75_997-74insG
NM_181829.2:c.1000-75_1000-74insG NP_861967.1:n.1000-75_1000-74insG
NM_181830.2:c.874-75_874-74insG NP_861968.1:n.874-75_874-74insG
NM_181831.2:c.874-75_874-74insG NP_861969.1:n.874-75_874-74insG
NM_181832.2:c.1123-75_1123-74insG NP_861970.1:n.1123-75_1123-74insG
NM_181833.2:c.448-21558_448-21557insG NP_861971.1:n.448-21558_448-21557insG
NR_156186.1:n.1682-75_1682-74insG
XM_017028809.2:c.1009-75_1009-74insG XP_016884298.1:n.1009-75_1009-74insG
XM_017028810.1:c.1009-75_1009-74insG XP_016884299.1:n.1009-75_1009-74insG
NM_000268.4:c.1123-75_1123-74insG MANE Select NP_000259.1:n.1123-75_1123-74insG
NM_181825.3:c.1123-75_1123-74insG NP_861546.1:n.1123-75_1123-74insG
NM_181828.3:c.997-75_997-74insG NP_861966.1:n.997-75_997-74insG
NM_181829.3:c.1000-75_1000-74insG NP_861967.1:n.1000-75_1000-74insG
NM_181830.3:c.874-75_874-74insG NP_861968.1:n.874-75_874-74insG
NM_181831.3:c.874-75_874-74insG NP_861969.1:n.874-75_874-74insG
NM_181832.3:c.1123-75_1123-74insG NP_861970.1:n.1123-75_1123-74insG
NR_156186.2:n.1605-75_1605-74insG
NM_181833.3:c.448-21558_448-21557insG NP_861971.1:n.448-21558_448-21557insG