Canonical Allele Identifier: CA2818684403

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29674992_29674993del , CM000684.2:g.29674992_29674993del	GRCh38
NC_000022.10:g.30070981_30070982del , CM000684.1:g.30070981_30070982del	GRCh37
NC_000022.9:g.28400981_28400982del	NCBI36
NG_009057.1:g.76437_76438del , LRG_511:g.76437_76438del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1311+51_1311+52del	ENSP00000354529.6:n.1311+51_1311+52del
ENST00000673312.2:c.*940+51_*940+52del	ENSP00000500186.2:n.*940+51_*940+52del
ENST00000338641.10:c.1446+51_1446+52del MANE Select	ENSP00000344666.5:n.1446+51_1446+52del
ENST00000361166.9:c.864+51_864+52del	ENSP00000354529.5:n.864+51_864+52del
ENST00000672461.1:c.1446+51_1446+52del	ENSP00000500919.1:n.1446+51_1446+52del
ENST00000672805.1:c.*1328+51_*1328+52del	ENSP00000500295.1:n.*1328+51_*1328+52del
ENST00000672896.1:c.1446+51_1446+52del	ENSP00000500117.1:n.1446+51_1446+52del
ENST00000673312.1:c.1465+51_1465+52del	ENSP00000500186.1:n.1465+51_1465+52del
ENST00000334961.11:c.1197+51_1197+52del	ENSP00000335652.7:n.1197+51_1197+52del
ENST00000338641.8:c.1446+51_1446+52del	ENSP00000344666.4:n.1446+51_1446+52del
ENST00000353887.8:c.1197+51_1197+52del	ENSP00000340626.4:n.1197+51_1197+52del
ENST00000361166.8:c.1446+51_1446+52del	ENSP00000354529.4:n.1446+51_1446+52del
ENST00000361452.8:c.1323+51_1323+52del	ENSP00000354897.4:n.1323+51_1323+52del
ENST00000361676.8:c.1320+51_1320+52del	ENSP00000355183.4:n.1320+51_1320+52del
ENST00000397789.3:c.1446+51_1446+52del	ENSP00000380891.3:n.1446+51_1446+52del
ENST00000403435.5:c.1359+51_1359+52del	ENSP00000384029.1:n.1359+51_1359+52del
ENST00000403999.7:c.1446+51_1446+52del	ENSP00000384797.3:n.1446+51_1446+52del
ENST00000413209.6:c.448-19760_448-19759del	ENSP00000409921.2:n.448-19760_448-19759del
ENST00000432151.5:c.628+51_628+52del	ENSP00000395885.1:n.628+51_628+52del
NM_000268.3:c.1446+51_1446+52del , LRG_511t1:c.1446+51_1446+52del	NP_000259.1:n.1446+51_1446+52del
NM_016418.5:c.1446+51_1446+52del , LRG_511t2:c.1446+51_1446+52del	NP_057502.2:n.1446+51_1446+52del
NM_181825.2:c.1446+51_1446+52del	NP_861546.1:n.1446+51_1446+52del
NM_181828.2:c.1320+51_1320+52del	NP_861966.1:n.1320+51_1320+52del
NM_181829.2:c.1323+51_1323+52del	NP_861967.1:n.1323+51_1323+52del
NM_181830.2:c.1197+51_1197+52del	NP_861968.1:n.1197+51_1197+52del
NM_181831.2:c.1197+51_1197+52del	NP_861969.1:n.1197+51_1197+52del
NM_181832.2:c.1446+51_1446+52del	NP_861970.1:n.1446+51_1446+52del
NM_181833.2:c.448-19760_448-19759del	NP_861971.1:n.448-19760_448-19759del
NR_156186.1:n.2005+51_2005+52del
XM_017028809.2:c.1332+51_1332+52del	XP_016884298.1:n.1332+51_1332+52del
XM_017028810.1:c.1332+51_1332+52del	XP_016884299.1:n.1332+51_1332+52del
NM_000268.4:c.1446+51_1446+52del MANE Select	NP_000259.1:n.1446+51_1446+52del
NM_181825.3:c.1446+51_1446+52del	NP_861546.1:n.1446+51_1446+52del
NM_181828.3:c.1320+51_1320+52del	NP_861966.1:n.1320+51_1320+52del
NM_181829.3:c.1323+51_1323+52del	NP_861967.1:n.1323+51_1323+52del
NM_181830.3:c.1197+51_1197+52del	NP_861968.1:n.1197+51_1197+52del
NM_181831.3:c.1197+51_1197+52del	NP_861969.1:n.1197+51_1197+52del
NM_181832.3:c.1446+51_1446+52del	NP_861970.1:n.1446+51_1446+52del
NR_156186.2:n.1928+51_1928+52del
NM_181833.3:c.448-19760_448-19759del	NP_861971.1:n.448-19760_448-19759del