Canonical Allele Identifier: CA2400683214
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29673190C= , CM000684.2:g.29673190C= GRCh38
NC_000022.10:g.30069179C= , CM000684.1:g.30069179C= GRCh37
NC_000022.9:g.28399179C= NCBI36
NG_009057.1:g.74635C= , LRG_511:g.74635C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361166.10:c.988-79C= ENSP00000354529.6:n.988-79C=
ENST00000673312.2:c.*617-79C= ENSP00000500186.2:n.*617-79C=
ENST00000338641.10:c.1123-79C= MANE Select ENSP00000344666.5:n.1123-79C=
ENST00000361166.9:c.541-79C= ENSP00000354529.5:n.541-79C=
ENST00000672461.1:c.1123-79C= ENSP00000500919.1:n.1123-79C=
ENST00000672805.1:c.*1005-79C= ENSP00000500295.1:n.*1005-79C=
ENST00000672896.1:c.1123-79C= ENSP00000500117.1:n.1123-79C=
ENST00000673312.1:c.1142-79C= ENSP00000500186.1:n.1142-79C=
ENST00000334961.11:c.874-79C= ENSP00000335652.7:n.874-79C=
ENST00000338641.8:c.1123-79C= ENSP00000344666.4:n.1123-79C=
ENST00000353887.8:c.874-79C= ENSP00000340626.4:n.874-79C=
ENST00000361166.8:c.1123-79C= ENSP00000354529.4:n.1123-79C=
ENST00000361452.8:c.1000-79C= ENSP00000354897.4:n.1000-79C=
ENST00000361676.8:c.997-79C= ENSP00000355183.4:n.997-79C=
ENST00000397789.3:c.1123-79C= ENSP00000380891.3:n.1123-79C=
ENST00000403435.5:c.1036-79C= ENSP00000384029.1:n.1036-79C=
ENST00000403999.7:c.1123-79C= ENSP00000384797.3:n.1123-79C=
ENST00000413209.6:c.448-21562C= ENSP00000409921.2:n.448-21562C=
ENST00000432151.5:c.523-1646C= ENSP00000395885.1:n.523-1646C=
NM_000268.3:c.1123-79C= , LRG_511t1:c.1123-79C= NP_000259.1:n.1123-79C=
NM_016418.5:c.1123-79C= , LRG_511t2:c.1123-79C= NP_057502.2:n.1123-79C=
NM_181825.2:c.1123-79C= NP_861546.1:n.1123-79C=
NM_181828.2:c.997-79C= NP_861966.1:n.997-79C=
NM_181829.2:c.1000-79C= NP_861967.1:n.1000-79C=
NM_181830.2:c.874-79C= NP_861968.1:n.874-79C=
NM_181831.2:c.874-79C= NP_861969.1:n.874-79C=
NM_181832.2:c.1123-79C= NP_861970.1:n.1123-79C=
NM_181833.2:c.448-21562C= NP_861971.1:n.448-21562C=
NR_156186.1:n.1682-79C=
XM_017028809.2:c.1009-79C= XP_016884298.1:n.1009-79C=
XM_017028810.1:c.1009-79C= XP_016884299.1:n.1009-79C=
NM_000268.4:c.1123-79C= MANE Select NP_000259.1:n.1123-79C=
NM_181825.3:c.1123-79C= NP_861546.1:n.1123-79C=
NM_181828.3:c.997-79C= NP_861966.1:n.997-79C=
NM_181829.3:c.1000-79C= NP_861967.1:n.1000-79C=
NM_181830.3:c.874-79C= NP_861968.1:n.874-79C=
NM_181831.3:c.874-79C= NP_861969.1:n.874-79C=
NM_181832.3:c.1123-79C= NP_861970.1:n.1123-79C=
NR_156186.2:n.1605-79C=
NM_181833.3:c.448-21562C= NP_861971.1:n.448-21562C=