Canonical Allele Identifier: CA2400675309

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29654670_29654671delinsAC , CM000684.2:g.29654670_29654671delinsAC	GRCh38
NC_000022.10:g.30050659_30050660delinsAC , CM000684.1:g.30050659_30050660delinsAC	GRCh37
NC_000022.9:g.28380659_28380660delinsAC	NCBI36
NG_009057.1:g.56115_56116delinsAC , LRG_511:g.56115_56116delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.461_462delinsAC	ENSP00000354529.6:p.Asp154=
ENST00000673312.2:c.461_462delinsAC	ENSP00000500186.2:p.Asp154=
ENST00000338641.10:c.461_462delinsAC MANE Select	ENSP00000344666.5:p.Asp154=
ENST00000361166.9:c.14_15delinsAC	ENSP00000354529.5:p.Asp5=
ENST00000672461.1:c.461_462delinsAC	ENSP00000500919.1:p.Asp154=
ENST00000672805.1:c.*343_*344delinsAC	ENSP00000500295.1:n.*343_*344delinsAC
ENST00000672896.1:c.461_462delinsAC	ENSP00000500117.1:p.Asp154=
ENST00000673312.1:c.374_375delinsAC	ENSP00000500186.1:p.Asp125=
ENST00000334961.11:c.212_213delinsAC	ENSP00000335652.7:p.Asp71=
ENST00000338641.8:c.461_462delinsAC	ENSP00000344666.4:p.Asp154=
ENST00000353887.8:c.212_213delinsAC	ENSP00000340626.4:p.Asp71=
ENST00000361166.8:c.461_462delinsAC	ENSP00000354529.4:p.Asp154=
ENST00000361452.8:c.338_339delinsAC	ENSP00000354897.4:p.Asp113=
ENST00000361676.8:c.335_336delinsAC	ENSP00000355183.4:p.Asp112=
ENST00000397789.3:c.461_462delinsAC	ENSP00000380891.3:p.Asp154=
ENST00000403435.5:c.461_462delinsAC	ENSP00000384029.1:p.Asp154=
ENST00000403999.7:c.461_462delinsAC	ENSP00000384797.3:p.Asp154=
ENST00000413209.6:c.447+12385_447+12386delinsAC	ENSP00000409921.2:n.447+12385_447+12386delinsAC
ENST00000432151.5:c.199-6535_199-6534delinsAC	ENSP00000395885.1:n.199-6535_199-6534delinsAC
NM_000268.3:c.461_462delinsAC , LRG_511t1:c.461_462delinsAC	NP_000259.1:p.Asp154=
NM_016418.5:c.461_462delinsAC , LRG_511t2:c.461_462delinsAC	NP_057502.2:p.Asp154=
NM_181825.2:c.461_462delinsAC	NP_861546.1:p.Asp154=
NM_181828.2:c.335_336delinsAC	NP_861966.1:p.Asp112=
NM_181829.2:c.338_339delinsAC	NP_861967.1:p.Asp113=
NM_181830.2:c.212_213delinsAC	NP_861968.1:p.Asp71=
NM_181831.2:c.212_213delinsAC	NP_861969.1:p.Asp71=
NM_181832.2:c.461_462delinsAC	NP_861970.1:p.Asp154=
NM_181833.2:c.447+12385_447+12386delinsAC	NP_861971.1:n.447+12385_447+12386delinsAC
NR_156186.1:n.1020_1021delinsAC
XM_017028809.2:c.347_348delinsAC	XP_016884298.1:p.Asp116=
XM_017028810.1:c.347_348delinsAC	XP_016884299.1:p.Asp116=
NM_000268.4:c.461_462delinsAC MANE Select	NP_000259.1:p.Asp154=
NM_181825.3:c.461_462delinsAC	NP_861546.1:p.Asp154=
NM_181828.3:c.335_336delinsAC	NP_861966.1:p.Asp112=
NM_181829.3:c.338_339delinsAC	NP_861967.1:p.Asp113=
NM_181830.3:c.212_213delinsAC	NP_861968.1:p.Asp71=
NM_181831.3:c.212_213delinsAC	NP_861969.1:p.Asp71=
NM_181832.3:c.461_462delinsAC	NP_861970.1:p.Asp154=
NR_156186.2:n.943_944delinsAC
NM_181833.3:c.447+12385_447+12386delinsAC	NP_861971.1:n.447+12385_447+12386delinsAC