Canonical Allele Identifier: CA2400675754

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29655656_29655663delinsAGAGCACC , CM000684.2:g.29655656_29655663delinsAGAGCACC	GRCh38
NC_000022.10:g.30051645_30051652delinsAGAGCACC , CM000684.1:g.30051645_30051652delinsAGAGCACC	GRCh37
NC_000022.9:g.28381645_28381652delinsAGAGCACC	NCBI36
NG_009057.1:g.57101_57108delinsAGAGCACC , LRG_511:g.57101_57108delinsAGAGCACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.579_586delinsAGAGCACC	ENSP00000354529.6:p.Ala193=
ENST00000673312.2:c.*73_*80delinsAGAGCACC	ENSP00000500186.2:n.*73_*80delinsAGAGCACC
ENST00000338641.10:c.579_586delinsAGAGCACC MANE Select	ENSP00000344666.5:p.Ala193=
ENST00000361166.9:c.132_139delinsAGAGCACC	ENSP00000354529.5:p.Ala44=
ENST00000672461.1:c.579_586delinsAGAGCACC	ENSP00000500919.1:p.Ala193=
ENST00000672805.1:c.*461_*468delinsAGAGCACC	ENSP00000500295.1:n.*461_*468delinsAGAGCACC
ENST00000672896.1:c.579_586delinsAGAGCACC	ENSP00000500117.1:p.Ala193=
ENST00000673312.1:c.598_605delinsAGAGCACC	ENSP00000500186.1:n.598_605delinsAGAGCACC
ENST00000334961.11:c.330_337delinsAGAGCACC	ENSP00000335652.7:p.Ala110=
ENST00000338641.8:c.579_586delinsAGAGCACC	ENSP00000344666.4:p.Ala193=
ENST00000353887.8:c.330_337delinsAGAGCACC	ENSP00000340626.4:p.Ala110=
ENST00000361166.8:c.579_586delinsAGAGCACC	ENSP00000354529.4:p.Ala193=
ENST00000361452.8:c.456_463delinsAGAGCACC	ENSP00000354897.4:p.Ala152=
ENST00000361676.8:c.453_460delinsAGAGCACC	ENSP00000355183.4:p.Ala151=
ENST00000397789.3:c.579_586delinsAGAGCACC	ENSP00000380891.3:p.Ala193=
ENST00000403435.5:c.579_586delinsAGAGCACC	ENSP00000384029.1:p.Ala193=
ENST00000403999.7:c.579_586delinsAGAGCACC	ENSP00000384797.3:p.Ala193=
ENST00000413209.6:c.447+13371_447+13378delinsAGAGCACC	ENSP00000409921.2:n.447+13371_447+13378delinsAGAGCACC
ENST00000432151.5:c.199-5549_199-5542delinsAGAGCACC	ENSP00000395885.1:n.199-5549_199-5542delinsAGAGCACC
NM_000268.3:c.579_586delinsAGAGCACC , LRG_511t1:c.579_586delinsAGAGCACC	NP_000259.1:p.Ala193=
NM_016418.5:c.579_586delinsAGAGCACC , LRG_511t2:c.579_586delinsAGAGCACC	NP_057502.2:p.Ala193=
NM_181825.2:c.579_586delinsAGAGCACC	NP_861546.1:p.Ala193=
NM_181828.2:c.453_460delinsAGAGCACC	NP_861966.1:p.Ala151=
NM_181829.2:c.456_463delinsAGAGCACC	NP_861967.1:p.Ala152=
NM_181830.2:c.330_337delinsAGAGCACC	NP_861968.1:p.Ala110=
NM_181831.2:c.330_337delinsAGAGCACC	NP_861969.1:p.Ala110=
NM_181832.2:c.579_586delinsAGAGCACC	NP_861970.1:p.Ala193=
NM_181833.2:c.447+13371_447+13378delinsAGAGCACC	NP_861971.1:n.447+13371_447+13378delinsAGAGCACC
NR_156186.1:n.1138_1145delinsAGAGCACC
XM_017028809.2:c.465_472delinsAGAGCACC	XP_016884298.1:p.Ala155=
XM_017028810.1:c.465_472delinsAGAGCACC	XP_016884299.1:p.Ala155=
NM_000268.4:c.579_586delinsAGAGCACC MANE Select	NP_000259.1:p.Ala193=
NM_181825.3:c.579_586delinsAGAGCACC	NP_861546.1:p.Ala193=
NM_181828.3:c.453_460delinsAGAGCACC	NP_861966.1:p.Ala151=
NM_181829.3:c.456_463delinsAGAGCACC	NP_861967.1:p.Ala152=
NM_181830.3:c.330_337delinsAGAGCACC	NP_861968.1:p.Ala110=
NM_181831.3:c.330_337delinsAGAGCACC	NP_861969.1:p.Ala110=
NM_181832.3:c.579_586delinsAGAGCACC	NP_861970.1:p.Ala193=
NR_156186.2:n.1061_1068delinsAGAGCACC
NM_181833.3:c.447+13371_447+13378delinsAGAGCACC	NP_861971.1:n.447+13371_447+13378delinsAGAGCACC