Canonical Allele Identifier: CA2580099512

Gene: NF2

Linked Data

• ClinVar Variation Id: 1774111
• ClinVar RCV Id: RCV002390028

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29678256del , CM000684.2:g.29678256del	GRCh38
NC_000022.10:g.30074245del , CM000684.1:g.30074245del	GRCh37
NC_000022.9:g.28404245del	NCBI36
NG_009057.1:g.79701del , LRG_511:g.79701del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1372del	ENSP00000354529.6:p.Asp458ThrfsTer12
ENST00000673312.2:c.*1001del	ENSP00000500186.2:n.*1001del
ENST00000338641.10:c.1507del MANE Select	ENSP00000344666.5:p.Asp503ThrfsTer12
ENST00000361166.9:c.925del	ENSP00000354529.5:p.Asp309ThrfsTer12
ENST00000672461.1:c.1507del	ENSP00000500919.1:p.Asp503ThrfsTer12
ENST00000672805.1:c.*1389del	ENSP00000500295.1:n.*1389del
ENST00000672896.1:c.1507del	ENSP00000500117.1:p.Asp503ThrfsTer12
ENST00000673312.1:c.1526del	ENSP00000500186.1:n.1526del
ENST00000334961.11:c.1258del	ENSP00000335652.7:p.Asp420ThrfsTer12
ENST00000338641.8:c.1507del	ENSP00000344666.4:p.Asp503ThrfsTer12
ENST00000353887.8:c.1258del	ENSP00000340626.4:p.Asp420ThrfsTer12
ENST00000361166.8:c.1507del	ENSP00000354529.4:p.Asp503ThrfsTer12
ENST00000361452.8:c.1384del	ENSP00000354897.4:p.Asp462ThrfsTer12
ENST00000361676.8:c.1381del	ENSP00000355183.4:p.Asp461ThrfsTer12
ENST00000397789.3:c.1507del	ENSP00000380891.3:p.Asp503ThrfsTer12
ENST00000403435.5:c.1420del	ENSP00000384029.1:p.Asp474ThrfsTer12
ENST00000403999.7:c.1507del	ENSP00000384797.3:p.Asp503ThrfsTer12
ENST00000413209.6:c.448-16496del	ENSP00000409921.2:n.448-16496del
ENST00000432151.5:c.*26del	ENSP00000395885.1:n.*26del
NM_000268.3:c.1507del , LRG_511t1:c.1507del	NP_000259.1:p.Asp503ThrfsTer12
NM_016418.5:c.1507del , LRG_511t2:c.1507del	NP_057502.2:p.Asp503ThrfsTer12
NM_181825.2:c.1507del	NP_861546.1:p.Asp503ThrfsTer12
NM_181828.2:c.1381del	NP_861966.1:p.Asp461ThrfsTer12
NM_181829.2:c.1384del	NP_861967.1:p.Asp462ThrfsTer12
NM_181830.2:c.1258del	NP_861968.1:p.Asp420ThrfsTer12
NM_181831.2:c.1258del	NP_861969.1:p.Asp420ThrfsTer12
NM_181832.2:c.1507del	NP_861970.1:p.Asp503ThrfsTer12
NM_181833.2:c.448-16496del	NP_861971.1:n.448-16496del
NR_156186.1:n.2066del
XM_017028809.2:c.1393del	XP_016884298.1:p.Asp465ThrfsTer12
XM_017028810.1:c.1393del	XP_016884299.1:p.Asp465ThrfsTer12
NM_000268.4:c.1507del MANE Select	NP_000259.1:p.Asp503ThrfsTer12
NM_181825.3:c.1507del	NP_861546.1:p.Asp503ThrfsTer12
NM_181828.3:c.1381del	NP_861966.1:p.Asp461ThrfsTer12
NM_181829.3:c.1384del	NP_861967.1:p.Asp462ThrfsTer12
NM_181830.3:c.1258del	NP_861968.1:p.Asp420ThrfsTer12
NM_181831.3:c.1258del	NP_861969.1:p.Asp420ThrfsTer12
NM_181832.3:c.1507del	NP_861970.1:p.Asp503ThrfsTer12
NR_156186.2:n.1989del
NM_181833.3:c.448-16496del	NP_861971.1:n.448-16496del