Canonical Allele Identifier: CA2656032813

Gene: NF2

Linked Data

• gnomAD v4: 22-29681410-CCTGATG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29681412_29681417del , CM000684.2:g.29681412_29681417del	GRCh38
NC_000022.10:g.30077401_30077406del , CM000684.1:g.30077401_30077406del	GRCh37
NC_000022.9:g.28407401_28407406del	NCBI36
NG_009057.1:g.82857_82862del , LRG_511:g.82857_82862del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1440-27_1440-22del	ENSP00000354529.6:n.1440-27_1440-22del
ENST00000673312.2:c.*1069-27_*1069-22del	ENSP00000500186.2:n.*1069-27_*1069-22del
ENST00000338641.10:c.1575-27_1575-22del MANE Select	ENSP00000344666.5:n.1575-27_1575-22del
ENST00000361166.9:c.993-27_993-22del	ENSP00000354529.5:n.993-27_993-22del
ENST00000672461.1:c.1575-27_1575-22del	ENSP00000500919.1:n.1575-27_1575-22del
ENST00000672805.1:c.*1457-27_*1457-22del	ENSP00000500295.1:n.*1457-27_*1457-22del
ENST00000672896.1:c.1575-27_1575-22del	ENSP00000500117.1:n.1575-27_1575-22del
ENST00000673312.1:c.1594-27_1594-22del	ENSP00000500186.1:n.1594-27_1594-22del
ENST00000334961.11:c.1326-27_1326-22del	ENSP00000335652.7:n.1326-27_1326-22del
ENST00000338641.8:c.1575-27_1575-22del	ENSP00000344666.4:n.1575-27_1575-22del
ENST00000353887.8:c.1326-27_1326-22del	ENSP00000340626.4:n.1326-27_1326-22del
ENST00000361166.8:c.1575-27_1575-22del	ENSP00000354529.4:n.1575-27_1575-22del
ENST00000361452.8:c.1452-27_1452-22del	ENSP00000354897.4:n.1452-27_1452-22del
ENST00000361676.8:c.1449-27_1449-22del	ENSP00000355183.4:n.1449-27_1449-22del
ENST00000397789.3:c.1575-27_1575-22del	ENSP00000380891.3:n.1575-27_1575-22del
ENST00000403435.5:c.1488-27_1488-22del	ENSP00000384029.1:n.1488-27_1488-22del
ENST00000403999.7:c.1575-27_1575-22del	ENSP00000384797.3:n.1575-27_1575-22del
ENST00000413209.6:c.448-13340_448-13335del	ENSP00000409921.2:n.448-13340_448-13335del
ENST00000432151.5:c.*93+3089_*93+3094del	ENSP00000395885.1:n.*93+3089_*93+3094del
NM_000268.3:c.1575-27_1575-22del , LRG_511t1:c.1575-27_1575-22del	NP_000259.1:n.1575-27_1575-22del
NM_016418.5:c.1575-27_1575-22del , LRG_511t2:c.1575-27_1575-22del	NP_057502.2:n.1575-27_1575-22del
NM_181825.2:c.1575-27_1575-22del	NP_861546.1:n.1575-27_1575-22del
NM_181828.2:c.1449-27_1449-22del	NP_861966.1:n.1449-27_1449-22del
NM_181829.2:c.1452-27_1452-22del	NP_861967.1:n.1452-27_1452-22del
NM_181830.2:c.1326-27_1326-22del	NP_861968.1:n.1326-27_1326-22del
NM_181831.2:c.1326-27_1326-22del	NP_861969.1:n.1326-27_1326-22del
NM_181832.2:c.1575-27_1575-22del	NP_861970.1:n.1575-27_1575-22del
NM_181833.2:c.448-13340_448-13335del	NP_861971.1:n.448-13340_448-13335del
NR_156186.1:n.2134-27_2134-22del
XM_017028809.2:c.1461-27_1461-22del	XP_016884298.1:n.1461-27_1461-22del
XM_017028810.1:c.1461-27_1461-22del	XP_016884299.1:n.1461-27_1461-22del
NM_000268.4:c.1575-27_1575-22del MANE Select	NP_000259.1:n.1575-27_1575-22del
NM_181825.3:c.1575-27_1575-22del	NP_861546.1:n.1575-27_1575-22del
NM_181828.3:c.1449-27_1449-22del	NP_861966.1:n.1449-27_1449-22del
NM_181829.3:c.1452-27_1452-22del	NP_861967.1:n.1452-27_1452-22del
NM_181830.3:c.1326-27_1326-22del	NP_861968.1:n.1326-27_1326-22del
NM_181831.3:c.1326-27_1326-22del	NP_861969.1:n.1326-27_1326-22del
NM_181832.3:c.1575-27_1575-22del	NP_861970.1:n.1575-27_1575-22del
NR_156186.2:n.2057-27_2057-22del
NM_181833.3:c.448-13340_448-13335del	NP_861971.1:n.448-13340_448-13335del