Canonical Allele Identifier: CA2400685387

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29678193_29678194delinsCA , CM000684.2:g.29678193_29678194delinsCA	GRCh38
NC_000022.10:g.30074182_30074183delinsCA , CM000684.1:g.30074182_30074183delinsCA	GRCh37
NC_000022.9:g.28404182_28404183delinsCA	NCBI36
NG_009057.1:g.79638_79639delinsCA , LRG_511:g.79638_79639delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1312-3_1312-2delinsCA	ENSP00000354529.6:n.1312-3_1312-2delinsCA
ENST00000673312.2:c.*941-3_*941-2delinsCA	ENSP00000500186.2:n.*941-3_*941-2delinsCA
ENST00000338641.10:c.1447-3_1447-2delinsCA MANE Select	ENSP00000344666.5:n.1447-3_1447-2delinsCA
ENST00000361166.9:c.865-3_865-2delinsCA	ENSP00000354529.5:n.865-3_865-2delinsCA
ENST00000672461.1:c.1447-3_1447-2delinsCA	ENSP00000500919.1:n.1447-3_1447-2delinsCA
ENST00000672805.1:c.*1329-3_*1329-2delinsCA	ENSP00000500295.1:n.*1329-3_*1329-2delinsCA
ENST00000672896.1:c.1447-3_1447-2delinsCA	ENSP00000500117.1:n.1447-3_1447-2delinsCA
ENST00000673312.1:c.1466-3_1466-2delinsCA	ENSP00000500186.1:n.1466-3_1466-2delinsCA
ENST00000334961.11:c.1198-3_1198-2delinsCA	ENSP00000335652.7:n.1198-3_1198-2delinsCA
ENST00000338641.8:c.1447-3_1447-2delinsCA	ENSP00000344666.4:n.1447-3_1447-2delinsCA
ENST00000353887.8:c.1198-3_1198-2delinsCA	ENSP00000340626.4:n.1198-3_1198-2delinsCA
ENST00000361166.8:c.1447-3_1447-2delinsCA	ENSP00000354529.4:n.1447-3_1447-2delinsCA
ENST00000361452.8:c.1324-3_1324-2delinsCA	ENSP00000354897.4:n.1324-3_1324-2delinsCA
ENST00000361676.8:c.1321-3_1321-2delinsCA	ENSP00000355183.4:n.1321-3_1321-2delinsCA
ENST00000397789.3:c.1447-3_1447-2delinsCA	ENSP00000380891.3:n.1447-3_1447-2delinsCA
ENST00000403435.5:c.1360-3_1360-2delinsCA	ENSP00000384029.1:n.1360-3_1360-2delinsCA
ENST00000403999.7:c.1447-3_1447-2delinsCA	ENSP00000384797.3:n.1447-3_1447-2delinsCA
ENST00000413209.6:c.448-16559_448-16558delinsCA	ENSP00000409921.2:n.448-16559_448-16558delinsCA
ENST00000432151.5:c.629-3_629-2delinsCA	ENSP00000395885.1:n.629-3_629-2delinsCA
NM_000268.3:c.1447-3_1447-2delinsCA , LRG_511t1:c.1447-3_1447-2delinsCA	NP_000259.1:n.1447-3_1447-2delinsCA
NM_016418.5:c.1447-3_1447-2delinsCA , LRG_511t2:c.1447-3_1447-2delinsCA	NP_057502.2:n.1447-3_1447-2delinsCA
NM_181825.2:c.1447-3_1447-2delinsCA	NP_861546.1:n.1447-3_1447-2delinsCA
NM_181828.2:c.1321-3_1321-2delinsCA	NP_861966.1:n.1321-3_1321-2delinsCA
NM_181829.2:c.1324-3_1324-2delinsCA	NP_861967.1:n.1324-3_1324-2delinsCA
NM_181830.2:c.1198-3_1198-2delinsCA	NP_861968.1:n.1198-3_1198-2delinsCA
NM_181831.2:c.1198-3_1198-2delinsCA	NP_861969.1:n.1198-3_1198-2delinsCA
NM_181832.2:c.1447-3_1447-2delinsCA	NP_861970.1:n.1447-3_1447-2delinsCA
NM_181833.2:c.448-16559_448-16558delinsCA	NP_861971.1:n.448-16559_448-16558delinsCA
NR_156186.1:n.2006-3_2006-2delinsCA
XM_017028809.2:c.1333-3_1333-2delinsCA	XP_016884298.1:n.1333-3_1333-2delinsCA
XM_017028810.1:c.1333-3_1333-2delinsCA	XP_016884299.1:n.1333-3_1333-2delinsCA
NM_000268.4:c.1447-3_1447-2delinsCA MANE Select	NP_000259.1:n.1447-3_1447-2delinsCA
NM_181825.3:c.1447-3_1447-2delinsCA	NP_861546.1:n.1447-3_1447-2delinsCA
NM_181828.3:c.1321-3_1321-2delinsCA	NP_861966.1:n.1321-3_1321-2delinsCA
NM_181829.3:c.1324-3_1324-2delinsCA	NP_861967.1:n.1324-3_1324-2delinsCA
NM_181830.3:c.1198-3_1198-2delinsCA	NP_861968.1:n.1198-3_1198-2delinsCA
NM_181831.3:c.1198-3_1198-2delinsCA	NP_861969.1:n.1198-3_1198-2delinsCA
NM_181832.3:c.1447-3_1447-2delinsCA	NP_861970.1:n.1447-3_1447-2delinsCA
NR_156186.2:n.1929-3_1929-2delinsCA
NM_181833.3:c.448-16559_448-16558delinsCA	NP_861971.1:n.448-16559_448-16558delinsCA