Canonical Allele Identifier: CA2695230514

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29678283dup , CM000684.2:g.29678283dup	GRCh38
NC_000022.10:g.30074272dup , CM000684.1:g.30074272dup	GRCh37
NC_000022.9:g.28404272dup	NCBI36
NG_009057.1:g.79728dup , LRG_511:g.79728dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.1399dup	ENSP00000354529.6:p.Thr467AsnfsTer2
ENST00000673312.2:c.*1028dup	ENSP00000500186.2:n.*1028dup
ENST00000338641.10:c.1534dup MANE Select	ENSP00000344666.5:p.Thr512AsnfsTer2
ENST00000361166.9:c.952dup	ENSP00000354529.5:p.Thr318AsnfsTer2
ENST00000672461.1:c.1534dup	ENSP00000500919.1:p.Thr512AsnfsTer2
ENST00000672805.1:c.*1416dup	ENSP00000500295.1:n.*1416dup
ENST00000672896.1:c.1534dup	ENSP00000500117.1:p.Thr512AsnfsTer2
ENST00000673312.1:c.1553dup	ENSP00000500186.1:n.1553dup
ENST00000334961.11:c.1285dup	ENSP00000335652.7:p.Thr429AsnfsTer2
ENST00000338641.8:c.1534dup	ENSP00000344666.4:p.Thr512AsnfsTer2
ENST00000353887.8:c.1285dup	ENSP00000340626.4:p.Thr429AsnfsTer2
ENST00000361166.8:c.1534dup	ENSP00000354529.4:p.Thr512AsnfsTer2
ENST00000361452.8:c.1411dup	ENSP00000354897.4:p.Thr471AsnfsTer2
ENST00000361676.8:c.1408dup	ENSP00000355183.4:p.Thr470AsnfsTer2
ENST00000397789.3:c.1534dup	ENSP00000380891.3:p.Thr512AsnfsTer2
ENST00000403435.5:c.1447dup	ENSP00000384029.1:p.Thr483AsnfsTer2
ENST00000403999.7:c.1534dup	ENSP00000384797.3:p.Thr512AsnfsTer2
ENST00000413209.6:c.448-16469dup	ENSP00000409921.2:n.448-16469dup
ENST00000432151.5:c.*53dup	ENSP00000395885.1:n.*53dup
NM_000268.3:c.1534dup , LRG_511t1:c.1534dup	NP_000259.1:p.Thr512AsnfsTer2
NM_016418.5:c.1534dup , LRG_511t2:c.1534dup	NP_057502.2:p.Thr512AsnfsTer2
NM_181825.2:c.1534dup	NP_861546.1:p.Thr512AsnfsTer2
NM_181828.2:c.1408dup	NP_861966.1:p.Thr470AsnfsTer2
NM_181829.2:c.1411dup	NP_861967.1:p.Thr471AsnfsTer2
NM_181830.2:c.1285dup	NP_861968.1:p.Thr429AsnfsTer2
NM_181831.2:c.1285dup	NP_861969.1:p.Thr429AsnfsTer2
NM_181832.2:c.1534dup	NP_861970.1:p.Thr512AsnfsTer2
NM_181833.2:c.448-16469dup	NP_861971.1:n.448-16469dup
NR_156186.1:n.2093dup
XM_017028809.2:c.1420dup	XP_016884298.1:p.Thr474AsnfsTer2
XM_017028810.1:c.1420dup	XP_016884299.1:p.Thr474AsnfsTer2
NM_000268.4:c.1534dup MANE Select	NP_000259.1:p.Thr512AsnfsTer2
NM_181825.3:c.1534dup	NP_861546.1:p.Thr512AsnfsTer2
NM_181828.3:c.1408dup	NP_861966.1:p.Thr470AsnfsTer2
NM_181829.3:c.1411dup	NP_861967.1:p.Thr471AsnfsTer2
NM_181830.3:c.1285dup	NP_861968.1:p.Thr429AsnfsTer2
NM_181831.3:c.1285dup	NP_861969.1:p.Thr429AsnfsTer2
NM_181832.3:c.1534dup	NP_861970.1:p.Thr512AsnfsTer2
NR_156186.2:n.2016dup
NM_181833.3:c.448-16469dup	NP_861971.1:n.448-16469dup