Canonical Allele Identifier: CA2400675676

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29655511_29655514delinsAATG , CM000684.2:g.29655511_29655514delinsAATG	GRCh38
NC_000022.10:g.30051500_30051503delinsAATG , CM000684.1:g.30051500_30051503delinsAATG	GRCh37
NC_000022.9:g.28381500_28381503delinsAATG	NCBI36
NG_009057.1:g.56956_56959delinsAATG , LRG_511:g.56956_56959delinsAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.517-83_517-80delinsAATG	ENSP00000354529.6:n.517-83_517-80delinsAATG
ENST00000673312.2:c.*11-83_*11-80delinsAATG	ENSP00000500186.2:n.*11-83_*11-80delinsAATG
ENST00000338641.10:c.517-83_517-80delinsAATG MANE Select	ENSP00000344666.5:n.517-83_517-80delinsAATG
ENST00000361166.9:c.70-83_70-80delinsAATG	ENSP00000354529.5:n.70-83_70-80delinsAATG
ENST00000672461.1:c.517-83_517-80delinsAATG	ENSP00000500919.1:n.517-83_517-80delinsAATG
ENST00000672805.1:c.*399-83_*399-80delinsAATG	ENSP00000500295.1:n.*399-83_*399-80delinsAATG
ENST00000672896.1:c.517-83_517-80delinsAATG	ENSP00000500117.1:n.517-83_517-80delinsAATG
ENST00000673312.1:c.536-83_536-80delinsAATG	ENSP00000500186.1:n.536-83_536-80delinsAATG
ENST00000334961.11:c.268-83_268-80delinsAATG	ENSP00000335652.7:n.268-83_268-80delinsAATG
ENST00000338641.8:c.517-83_517-80delinsAATG	ENSP00000344666.4:n.517-83_517-80delinsAATG
ENST00000353887.8:c.268-83_268-80delinsAATG	ENSP00000340626.4:n.268-83_268-80delinsAATG
ENST00000361166.8:c.517-83_517-80delinsAATG	ENSP00000354529.4:n.517-83_517-80delinsAATG
ENST00000361452.8:c.394-83_394-80delinsAATG	ENSP00000354897.4:n.394-83_394-80delinsAATG
ENST00000361676.8:c.391-83_391-80delinsAATG	ENSP00000355183.4:n.391-83_391-80delinsAATG
ENST00000397789.3:c.517-83_517-80delinsAATG	ENSP00000380891.3:n.517-83_517-80delinsAATG
ENST00000403435.5:c.517-83_517-80delinsAATG	ENSP00000384029.1:n.517-83_517-80delinsAATG
ENST00000403999.7:c.517-83_517-80delinsAATG	ENSP00000384797.3:n.517-83_517-80delinsAATG
ENST00000413209.6:c.447+13226_447+13229delinsAATG	ENSP00000409921.2:n.447+13226_447+13229delinsAATG
ENST00000432151.5:c.199-5694_199-5691delinsAATG	ENSP00000395885.1:n.199-5694_199-5691delinsAATG
NM_000268.3:c.517-83_517-80delinsAATG , LRG_511t1:c.517-83_517-80delinsAATG	NP_000259.1:n.517-83_517-80delinsAATG
NM_016418.5:c.517-83_517-80delinsAATG , LRG_511t2:c.517-83_517-80delinsAATG	NP_057502.2:n.517-83_517-80delinsAATG
NM_181825.2:c.517-83_517-80delinsAATG	NP_861546.1:n.517-83_517-80delinsAATG
NM_181828.2:c.391-83_391-80delinsAATG	NP_861966.1:n.391-83_391-80delinsAATG
NM_181829.2:c.394-83_394-80delinsAATG	NP_861967.1:n.394-83_394-80delinsAATG
NM_181830.2:c.268-83_268-80delinsAATG	NP_861968.1:n.268-83_268-80delinsAATG
NM_181831.2:c.268-83_268-80delinsAATG	NP_861969.1:n.268-83_268-80delinsAATG
NM_181832.2:c.517-83_517-80delinsAATG	NP_861970.1:n.517-83_517-80delinsAATG
NM_181833.2:c.447+13226_447+13229delinsAATG	NP_861971.1:n.447+13226_447+13229delinsAATG
NR_156186.1:n.1076-83_1076-80delinsAATG
XM_017028809.2:c.403-83_403-80delinsAATG	XP_016884298.1:n.403-83_403-80delinsAATG
XM_017028810.1:c.403-83_403-80delinsAATG	XP_016884299.1:n.403-83_403-80delinsAATG
NM_000268.4:c.517-83_517-80delinsAATG MANE Select	NP_000259.1:n.517-83_517-80delinsAATG
NM_181825.3:c.517-83_517-80delinsAATG	NP_861546.1:n.517-83_517-80delinsAATG
NM_181828.3:c.391-83_391-80delinsAATG	NP_861966.1:n.391-83_391-80delinsAATG
NM_181829.3:c.394-83_394-80delinsAATG	NP_861967.1:n.394-83_394-80delinsAATG
NM_181830.3:c.268-83_268-80delinsAATG	NP_861968.1:n.268-83_268-80delinsAATG
NM_181831.3:c.268-83_268-80delinsAATG	NP_861969.1:n.268-83_268-80delinsAATG
NM_181832.3:c.517-83_517-80delinsAATG	NP_861970.1:n.517-83_517-80delinsAATG
NR_156186.2:n.999-83_999-80delinsAATG
NM_181833.3:c.447+13226_447+13229delinsAATG	NP_861971.1:n.447+13226_447+13229delinsAATG