Canonical Allele Identifier: CA2695230639

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29655597dup , CM000684.2:g.29655597dup	GRCh38
NC_000022.10:g.30051586dup , CM000684.1:g.30051586dup	GRCh37
NC_000022.9:g.28381586dup	NCBI36
NG_009057.1:g.57042dup , LRG_511:g.57042dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.520dup	ENSP00000354529.6:p.Ile174AsnfsTer29
ENST00000673312.2:c.*14dup	ENSP00000500186.2:n.*14dup
ENST00000338641.10:c.520dup MANE Select	ENSP00000344666.5:p.Ile174AsnfsTer29
ENST00000361166.9:c.73dup	ENSP00000354529.5:p.Ile25AsnfsTer29
ENST00000672461.1:c.520dup	ENSP00000500919.1:p.Ile174AsnfsTer29
ENST00000672805.1:c.*402dup	ENSP00000500295.1:n.*402dup
ENST00000672896.1:c.520dup	ENSP00000500117.1:p.Ile174AsnfsTer29
ENST00000673312.1:c.539dup	ENSP00000500186.1:n.539dup
ENST00000334961.11:c.271dup	ENSP00000335652.7:p.Ile91AsnfsTer29
ENST00000338641.8:c.520dup	ENSP00000344666.4:p.Ile174AsnfsTer29
ENST00000353887.8:c.271dup	ENSP00000340626.4:p.Ile91AsnfsTer29
ENST00000361166.8:c.520dup	ENSP00000354529.4:p.Ile174AsnfsTer29
ENST00000361452.8:c.397dup	ENSP00000354897.4:p.Ile133AsnfsTer29
ENST00000361676.8:c.394dup	ENSP00000355183.4:p.Ile132AsnfsTer29
ENST00000397789.3:c.520dup	ENSP00000380891.3:p.Ile174AsnfsTer29
ENST00000403435.5:c.520dup	ENSP00000384029.1:p.Ile174AsnfsTer29
ENST00000403999.7:c.520dup	ENSP00000384797.3:p.Ile174AsnfsTer29
ENST00000413209.6:c.447+13312dup	ENSP00000409921.2:n.447+13312dup
ENST00000432151.5:c.199-5608dup	ENSP00000395885.1:n.199-5608dup
NM_000268.3:c.520dup , LRG_511t1:c.520dup	NP_000259.1:p.Ile174AsnfsTer29
NM_016418.5:c.520dup , LRG_511t2:c.520dup	NP_057502.2:p.Ile174AsnfsTer29
NM_181825.2:c.520dup	NP_861546.1:p.Ile174AsnfsTer29
NM_181828.2:c.394dup	NP_861966.1:p.Ile132AsnfsTer29
NM_181829.2:c.397dup	NP_861967.1:p.Ile133AsnfsTer29
NM_181830.2:c.271dup	NP_861968.1:p.Ile91AsnfsTer29
NM_181831.2:c.271dup	NP_861969.1:p.Ile91AsnfsTer29
NM_181832.2:c.520dup	NP_861970.1:p.Ile174AsnfsTer29
NM_181833.2:c.447+13312dup	NP_861971.1:n.447+13312dup
NR_156186.1:n.1079dup
XM_017028809.2:c.406dup	XP_016884298.1:p.Ile136AsnfsTer29
XM_017028810.1:c.406dup	XP_016884299.1:p.Ile136AsnfsTer29
NM_000268.4:c.520dup MANE Select	NP_000259.1:p.Ile174AsnfsTer29
NM_181825.3:c.520dup	NP_861546.1:p.Ile174AsnfsTer29
NM_181828.3:c.394dup	NP_861966.1:p.Ile132AsnfsTer29
NM_181829.3:c.397dup	NP_861967.1:p.Ile133AsnfsTer29
NM_181830.3:c.271dup	NP_861968.1:p.Ile91AsnfsTer29
NM_181831.3:c.271dup	NP_861969.1:p.Ile91AsnfsTer29
NM_181832.3:c.520dup	NP_861970.1:p.Ile174AsnfsTer29
NR_156186.2:n.1002dup
NM_181833.3:c.447+13312dup	NP_861971.1:n.447+13312dup