Canonical Allele Identifier: CA2400675211

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29654382_29654383delinsGT , CM000684.2:g.29654382_29654383delinsGT	GRCh38
NC_000022.10:g.30050371_30050372delinsGT , CM000684.1:g.30050371_30050372delinsGT	GRCh37
NC_000022.9:g.28380371_28380372delinsGT	NCBI36
NG_009057.1:g.55827_55828delinsGT , LRG_511:g.55827_55828delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.448-275_448-274delinsGT	ENSP00000354529.6:n.448-275_448-274delinsGT
ENST00000673312.2:c.448-275_448-274delinsGT	ENSP00000500186.2:n.448-275_448-274delinsGT
ENST00000338641.10:c.448-275_448-274delinsGT MANE Select	ENSP00000344666.5:n.448-275_448-274delinsGT
ENST00000672461.1:c.448-275_448-274delinsGT	ENSP00000500919.1:n.448-275_448-274delinsGT
ENST00000672805.1:c.*330-275_*330-274delinsGT	ENSP00000500295.1:n.*330-275_*330-274delinsGT
ENST00000672896.1:c.448-275_448-274delinsGT	ENSP00000500117.1:n.448-275_448-274delinsGT
ENST00000673312.1:c.361-275_361-274delinsGT	ENSP00000500186.1:n.361-275_361-274delinsGT
ENST00000334961.11:c.199-275_199-274delinsGT	ENSP00000335652.7:n.199-275_199-274delinsGT
ENST00000338641.8:c.448-275_448-274delinsGT	ENSP00000344666.4:n.448-275_448-274delinsGT
ENST00000353887.8:c.199-275_199-274delinsGT	ENSP00000340626.4:n.199-275_199-274delinsGT
ENST00000361166.8:c.448-275_448-274delinsGT	ENSP00000354529.4:n.448-275_448-274delinsGT
ENST00000361452.8:c.325-275_325-274delinsGT	ENSP00000354897.4:n.325-275_325-274delinsGT
ENST00000361676.8:c.322-275_322-274delinsGT	ENSP00000355183.4:n.322-275_322-274delinsGT
ENST00000397789.3:c.448-275_448-274delinsGT	ENSP00000380891.3:n.448-275_448-274delinsGT
ENST00000403435.5:c.448-275_448-274delinsGT	ENSP00000384029.1:n.448-275_448-274delinsGT
ENST00000403999.7:c.448-275_448-274delinsGT	ENSP00000384797.3:n.448-275_448-274delinsGT
ENST00000413209.6:c.447+12097_447+12098delinsGT	ENSP00000409921.2:n.447+12097_447+12098delinsGT
ENST00000432151.5:c.199-6823_199-6822delinsGT	ENSP00000395885.1:n.199-6823_199-6822delinsGT
NM_000268.3:c.448-275_448-274delinsGT , LRG_511t1:c.448-275_448-274delinsGT	NP_000259.1:n.448-275_448-274delinsGT
NM_016418.5:c.448-275_448-274delinsGT , LRG_511t2:c.448-275_448-274delinsGT	NP_057502.2:n.448-275_448-274delinsGT
NM_181825.2:c.448-275_448-274delinsGT	NP_861546.1:n.448-275_448-274delinsGT
NM_181828.2:c.322-275_322-274delinsGT	NP_861966.1:n.322-275_322-274delinsGT
NM_181829.2:c.325-275_325-274delinsGT	NP_861967.1:n.325-275_325-274delinsGT
NM_181830.2:c.199-275_199-274delinsGT	NP_861968.1:n.199-275_199-274delinsGT
NM_181831.2:c.199-275_199-274delinsGT	NP_861969.1:n.199-275_199-274delinsGT
NM_181832.2:c.448-275_448-274delinsGT	NP_861970.1:n.448-275_448-274delinsGT
NM_181833.2:c.447+12097_447+12098delinsGT	NP_861971.1:n.447+12097_447+12098delinsGT
NR_156186.1:n.1007-275_1007-274delinsGT
XM_017028809.2:c.334-275_334-274delinsGT	XP_016884298.1:n.334-275_334-274delinsGT
XM_017028810.1:c.334-275_334-274delinsGT	XP_016884299.1:n.334-275_334-274delinsGT
NM_000268.4:c.448-275_448-274delinsGT MANE Select	NP_000259.1:n.448-275_448-274delinsGT
NM_181825.3:c.448-275_448-274delinsGT	NP_861546.1:n.448-275_448-274delinsGT
NM_181828.3:c.322-275_322-274delinsGT	NP_861966.1:n.322-275_322-274delinsGT
NM_181829.3:c.325-275_325-274delinsGT	NP_861967.1:n.325-275_325-274delinsGT
NM_181830.3:c.199-275_199-274delinsGT	NP_861968.1:n.199-275_199-274delinsGT
NM_181831.3:c.199-275_199-274delinsGT	NP_861969.1:n.199-275_199-274delinsGT
NM_181832.3:c.448-275_448-274delinsGT	NP_861970.1:n.448-275_448-274delinsGT
NR_156186.2:n.930-275_930-274delinsGT
NM_181833.3:c.447+12097_447+12098delinsGT	NP_861971.1:n.447+12097_447+12098delinsGT