Canonical Allele Identifier: CA2400683989

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29674949_29674950delinsTG , CM000684.2:g.29674949_29674950delinsTG	GRCh38
NC_000022.10:g.30070938_30070939delinsTG , CM000684.1:g.30070938_30070939delinsTG	GRCh37
NC_000022.9:g.28400938_28400939delinsTG	NCBI36
NG_009057.1:g.76394_76395delinsTG , LRG_511:g.76394_76395delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1311+8_1311+9delinsTG	ENSP00000354529.6:n.1311+8_1311+9delinsTG
ENST00000673312.2:c.*940+8_*940+9delinsTG	ENSP00000500186.2:n.*940+8_*940+9delinsTG
ENST00000338641.10:c.1446+8_1446+9delinsTG MANE Select	ENSP00000344666.5:n.1446+8_1446+9delinsTG
ENST00000361166.9:c.864+8_864+9delinsTG	ENSP00000354529.5:n.864+8_864+9delinsTG
ENST00000672461.1:c.1446+8_1446+9delinsTG	ENSP00000500919.1:n.1446+8_1446+9delinsTG
ENST00000672805.1:c.*1328+8_*1328+9delinsTG	ENSP00000500295.1:n.*1328+8_*1328+9delinsTG
ENST00000672896.1:c.1446+8_1446+9delinsTG	ENSP00000500117.1:n.1446+8_1446+9delinsTG
ENST00000673312.1:c.1465+8_1465+9delinsTG	ENSP00000500186.1:n.1465+8_1465+9delinsTG
ENST00000334961.11:c.1197+8_1197+9delinsTG	ENSP00000335652.7:n.1197+8_1197+9delinsTG
ENST00000338641.8:c.1446+8_1446+9delinsTG	ENSP00000344666.4:n.1446+8_1446+9delinsTG
ENST00000353887.8:c.1197+8_1197+9delinsTG	ENSP00000340626.4:n.1197+8_1197+9delinsTG
ENST00000361166.8:c.1446+8_1446+9delinsTG	ENSP00000354529.4:n.1446+8_1446+9delinsTG
ENST00000361452.8:c.1323+8_1323+9delinsTG	ENSP00000354897.4:n.1323+8_1323+9delinsTG
ENST00000361676.8:c.1320+8_1320+9delinsTG	ENSP00000355183.4:n.1320+8_1320+9delinsTG
ENST00000397789.3:c.1446+8_1446+9delinsTG	ENSP00000380891.3:n.1446+8_1446+9delinsTG
ENST00000403435.5:c.1359+8_1359+9delinsTG	ENSP00000384029.1:n.1359+8_1359+9delinsTG
ENST00000403999.7:c.1446+8_1446+9delinsTG	ENSP00000384797.3:n.1446+8_1446+9delinsTG
ENST00000413209.6:c.448-19803_448-19802delinsTG	ENSP00000409921.2:n.448-19803_448-19802delinsTG
ENST00000432151.5:c.628+8_628+9delinsTG	ENSP00000395885.1:n.628+8_628+9delinsTG
NM_000268.3:c.1446+8_1446+9delinsTG , LRG_511t1:c.1446+8_1446+9delinsTG	NP_000259.1:n.1446+8_1446+9delinsTG
NM_016418.5:c.1446+8_1446+9delinsTG , LRG_511t2:c.1446+8_1446+9delinsTG	NP_057502.2:n.1446+8_1446+9delinsTG
NM_181825.2:c.1446+8_1446+9delinsTG	NP_861546.1:n.1446+8_1446+9delinsTG
NM_181828.2:c.1320+8_1320+9delinsTG	NP_861966.1:n.1320+8_1320+9delinsTG
NM_181829.2:c.1323+8_1323+9delinsTG	NP_861967.1:n.1323+8_1323+9delinsTG
NM_181830.2:c.1197+8_1197+9delinsTG	NP_861968.1:n.1197+8_1197+9delinsTG
NM_181831.2:c.1197+8_1197+9delinsTG	NP_861969.1:n.1197+8_1197+9delinsTG
NM_181832.2:c.1446+8_1446+9delinsTG	NP_861970.1:n.1446+8_1446+9delinsTG
NM_181833.2:c.448-19803_448-19802delinsTG	NP_861971.1:n.448-19803_448-19802delinsTG
NR_156186.1:n.2005+8_2005+9delinsTG
XM_017028809.2:c.1332+8_1332+9delinsTG	XP_016884298.1:n.1332+8_1332+9delinsTG
XM_017028810.1:c.1332+8_1332+9delinsTG	XP_016884299.1:n.1332+8_1332+9delinsTG
NM_000268.4:c.1446+8_1446+9delinsTG MANE Select	NP_000259.1:n.1446+8_1446+9delinsTG
NM_181825.3:c.1446+8_1446+9delinsTG	NP_861546.1:n.1446+8_1446+9delinsTG
NM_181828.3:c.1320+8_1320+9delinsTG	NP_861966.1:n.1320+8_1320+9delinsTG
NM_181829.3:c.1323+8_1323+9delinsTG	NP_861967.1:n.1323+8_1323+9delinsTG
NM_181830.3:c.1197+8_1197+9delinsTG	NP_861968.1:n.1197+8_1197+9delinsTG
NM_181831.3:c.1197+8_1197+9delinsTG	NP_861969.1:n.1197+8_1197+9delinsTG
NM_181832.3:c.1446+8_1446+9delinsTG	NP_861970.1:n.1446+8_1446+9delinsTG
NR_156186.2:n.1928+8_1928+9delinsTG
NM_181833.3:c.448-19803_448-19802delinsTG	NP_861971.1:n.448-19803_448-19802delinsTG