Canonical Allele Identifier: CA2400693455

Gene: NF2

Linked Data

• dbSNP Id: rs2067577983

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29697238_29697239insGGGACAGGGCGTAGGAGCTGT , CM000684.2:g.29697238_29697239insGGGACAGGGCGTAGGAGCTGT	GRCh38
NC_000022.10:g.30093227_30093228insGGGACAGGGCGTAGGAGCTGT , CM000684.1:g.30093227_30093228insGGGACAGGGCGTAGGAGCTGT	GRCh37
NC_000022.9:g.28423227_28423228insGGGACAGGGCGTAGGAGCTGT	NCBI36
NG_009057.1:g.98683_98684insGGGACAGGGCGTAGGAGCTGT , LRG_511:g.98683_98684insGGGACAGGGCGTAGGAGCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*2436_*2437insGGGACAGGGCGTAGGAGCTGT MANE Select	ENSP00000344666.5:n.*2436_*2437insGGGACAGGGCGTAGGAGCTGT
ENST00000672461.1:c.*502-23_*502-22insGGGACAGGGCGTAGGAGCTGT	ENSP00000500919.1:n.*502-23_*502-22insGGGACAGGGCGTAGGAGCTGT
ENST00000672896.1:c.*2496_*2497insGGGACAGGGCGTAGGAGCTGT	ENSP00000500117.1:n.*2496_*2497insGGGACAGGGCGTAGGAGCTGT
ENST00000338641.8:c.*2436_*2437insGGGACAGGGCGTAGGAGCTGT	ENSP00000344666.4:n.*2436_*2437insGGGACAGGGCGTAGGAGCTGT
ENST00000361452.8:c.*2496_*2497insGGGACAGGGCGTAGGAGCTGT	ENSP00000354897.4:n.*2496_*2497insGGGACAGGGCGTAGGAGCTGT
ENST00000413209.6:c.*2436_*2437insGGGACAGGGCGTAGGAGCTGT	ENSP00000409921.2:n.*2436_*2437insGGGACAGGGCGTAGGAGCTGT
NM_000268.3:c.*2436_*2437insGGGACAGGGCGTAGGAGCTGT , LRG_511t1:c.*2436_*2437insGGGACAGGGCGTAGGAGCTGT	NP_000259.1:n.*2436_*2437insGGGACAGGGCGTAGGAGCTGT
NM_016418.5:c.*2496_*2497insGGGACAGGGCGTAGGAGCTGT , LRG_511t2:c.*2496_*2497insGGGACAGGGCGTAGGAGCTGT	NP_057502.2:n.*2496_*2497insGGGACAGGGCGTAGGAGCTGT
NM_181828.2:c.*2496_*2497insGGGACAGGGCGTAGGAGCTGT	NP_861966.1:n.*2496_*2497insGGGACAGGGCGTAGGAGCTGT
NM_181829.2:c.*2496_*2497insGGGACAGGGCGTAGGAGCTGT	NP_861967.1:n.*2496_*2497insGGGACAGGGCGTAGGAGCTGT
NM_181830.2:c.*2496_*2497insGGGACAGGGCGTAGGAGCTGT	NP_861968.1:n.*2496_*2497insGGGACAGGGCGTAGGAGCTGT
NM_181832.2:c.*2511_*2512insGGGACAGGGCGTAGGAGCTGT	NP_861970.1:n.*2511_*2512insGGGACAGGGCGTAGGAGCTGT
NM_181833.2:c.*2436_*2437insGGGACAGGGCGTAGGAGCTGT	NP_861971.1:n.*2436_*2437insGGGACAGGGCGTAGGAGCTGT
NR_156186.1:n.4783_4784insGGGACAGGGCGTAGGAGCTGT
XM_017028810.1:c.*2496_*2497insGGGACAGGGCGTAGGAGCTGT	XP_016884299.1:n.*2496_*2497insGGGACAGGGCGTAGGAGCTGT
NM_000268.4:c.*2436_*2437insGGGACAGGGCGTAGGAGCTGT MANE Select	NP_000259.1:n.*2436_*2437insGGGACAGGGCGTAGGAGCTGT
NM_181828.3:c.*2496_*2497insGGGACAGGGCGTAGGAGCTGT	NP_861966.1:n.*2496_*2497insGGGACAGGGCGTAGGAGCTGT
NM_181829.3:c.*2496_*2497insGGGACAGGGCGTAGGAGCTGT	NP_861967.1:n.*2496_*2497insGGGACAGGGCGTAGGAGCTGT
NM_181830.3:c.*2496_*2497insGGGACAGGGCGTAGGAGCTGT	NP_861968.1:n.*2496_*2497insGGGACAGGGCGTAGGAGCTGT
NM_181832.3:c.*2511_*2512insGGGACAGGGCGTAGGAGCTGT	NP_861970.1:n.*2511_*2512insGGGACAGGGCGTAGGAGCTGT
NR_156186.2:n.4706_4707insGGGACAGGGCGTAGGAGCTGT
NM_181833.3:c.*2436_*2437insGGGACAGGGCGTAGGAGCTGT	NP_861971.1:n.*2436_*2437insGGGACAGGGCGTAGGAGCTGT