Canonical Allele Identifier: CA514184930

Gene: NF2

Linked Data

• COSMIC: COSM22253
• MyVariant Identifiers: chr22:g.30067903del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29671914del , CM000684.2:g.29671914del	GRCh38
NC_000022.10:g.30067903del , CM000684.1:g.30067903del	GRCh37
NC_000022.9:g.28397903del	NCBI36
NG_009057.1:g.73359del , LRG_511:g.73359del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.953del	ENSP00000354529.6:p.Met318ArgfsTer12
ENST00000673312.2:c.*582del	ENSP00000500186.2:n.*582del
ENST00000338641.10:c.1088del MANE Select	ENSP00000344666.5:p.Met363ArgfsTer12
ENST00000361166.9:c.506del	ENSP00000354529.5:p.Met169ArgfsTer12
ENST00000672461.1:c.1088del	ENSP00000500919.1:p.Met363ArgfsTer12
ENST00000672805.1:c.*970del	ENSP00000500295.1:n.*970del
ENST00000672896.1:c.1088del	ENSP00000500117.1:p.Met363ArgfsTer12
ENST00000673312.1:c.1107del	ENSP00000500186.1:n.1107del
ENST00000334961.11:c.839del	ENSP00000335652.7:p.Met280ArgfsTer12
ENST00000338641.8:c.1088del	ENSP00000344666.4:p.Met363ArgfsTer12
ENST00000353887.8:c.839del	ENSP00000340626.4:p.Met280ArgfsTer12
ENST00000361166.8:c.1088del	ENSP00000354529.4:p.Met363ArgfsTer12
ENST00000361452.8:c.965del	ENSP00000354897.4:p.Met322ArgfsTer12
ENST00000361676.8:c.962del	ENSP00000355183.4:p.Met321ArgfsTer12
ENST00000397789.3:c.1088del	ENSP00000380891.3:p.Met363ArgfsTer12
ENST00000403435.5:c.1001del	ENSP00000384029.1:p.Met334ArgfsTer12
ENST00000403999.7:c.1088del	ENSP00000384797.3:p.Met363ArgfsTer12
ENST00000413209.6:c.448-22838del	ENSP00000409921.2:n.448-22838del
ENST00000432151.5:c.523-2922del	ENSP00000395885.1:n.523-2922del
NM_000268.3:c.1088del , LRG_511t1:c.1088del	NP_000259.1:p.Met363ArgfsTer12
NM_016418.5:c.1088del , LRG_511t2:c.1088del	NP_057502.2:p.Met363ArgfsTer12
NM_181825.2:c.1088del	NP_861546.1:p.Met363ArgfsTer12
NM_181828.2:c.962del	NP_861966.1:p.Met321ArgfsTer12
NM_181829.2:c.965del	NP_861967.1:p.Met322ArgfsTer12
NM_181830.2:c.839del	NP_861968.1:p.Met280ArgfsTer12
NM_181831.2:c.839del	NP_861969.1:p.Met280ArgfsTer12
NM_181832.2:c.1088del	NP_861970.1:p.Met363ArgfsTer12
NM_181833.2:c.448-22838del	NP_861971.1:n.448-22838del
NR_156186.1:n.1647del
XM_017028809.2:c.974del	XP_016884298.1:p.Met325ArgfsTer12
XM_017028810.1:c.974del	XP_016884299.1:p.Met325ArgfsTer12
NM_000268.4:c.1088del MANE Select	NP_000259.1:p.Met363ArgfsTer12
NM_181825.3:c.1088del	NP_861546.1:p.Met363ArgfsTer12
NM_181828.3:c.962del	NP_861966.1:p.Met321ArgfsTer12
NM_181829.3:c.965del	NP_861967.1:p.Met322ArgfsTer12
NM_181830.3:c.839del	NP_861968.1:p.Met280ArgfsTer12
NM_181831.3:c.839del	NP_861969.1:p.Met280ArgfsTer12
NM_181832.3:c.1088del	NP_861970.1:p.Met363ArgfsTer12
NR_156186.2:n.1570del
NM_181833.3:c.448-22838del	NP_861971.1:n.448-22838del