Canonical Allele Identifier: CA2656032802

Gene: NF2

Linked Data

• gnomAD v4: 22-29681395-ACTGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29681399_29681402del , CM000684.2:g.29681399_29681402del	GRCh38
NC_000022.10:g.30077388_30077391del , CM000684.1:g.30077388_30077391del	GRCh37
NC_000022.9:g.28407388_28407391del	NCBI36
NG_009057.1:g.82844_82847del , LRG_511:g.82844_82847del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1440-40_1440-37del	ENSP00000354529.6:n.1440-40_1440-37del
ENST00000673312.2:c.*1069-40_*1069-37del	ENSP00000500186.2:n.*1069-40_*1069-37del
ENST00000338641.10:c.1575-40_1575-37del MANE Select	ENSP00000344666.5:n.1575-40_1575-37del
ENST00000361166.9:c.993-40_993-37del	ENSP00000354529.5:n.993-40_993-37del
ENST00000672461.1:c.1575-40_1575-37del	ENSP00000500919.1:n.1575-40_1575-37del
ENST00000672805.1:c.*1457-40_*1457-37del	ENSP00000500295.1:n.*1457-40_*1457-37del
ENST00000672896.1:c.1575-40_1575-37del	ENSP00000500117.1:n.1575-40_1575-37del
ENST00000673312.1:c.1594-40_1594-37del	ENSP00000500186.1:n.1594-40_1594-37del
ENST00000334961.11:c.1326-40_1326-37del	ENSP00000335652.7:n.1326-40_1326-37del
ENST00000338641.8:c.1575-40_1575-37del	ENSP00000344666.4:n.1575-40_1575-37del
ENST00000353887.8:c.1326-40_1326-37del	ENSP00000340626.4:n.1326-40_1326-37del
ENST00000361166.8:c.1575-40_1575-37del	ENSP00000354529.4:n.1575-40_1575-37del
ENST00000361452.8:c.1452-40_1452-37del	ENSP00000354897.4:n.1452-40_1452-37del
ENST00000361676.8:c.1449-40_1449-37del	ENSP00000355183.4:n.1449-40_1449-37del
ENST00000397789.3:c.1575-40_1575-37del	ENSP00000380891.3:n.1575-40_1575-37del
ENST00000403435.5:c.1488-40_1488-37del	ENSP00000384029.1:n.1488-40_1488-37del
ENST00000403999.7:c.1575-40_1575-37del	ENSP00000384797.3:n.1575-40_1575-37del
ENST00000413209.6:c.448-13353_448-13350del	ENSP00000409921.2:n.448-13353_448-13350del
ENST00000432151.5:c.*93+3076_*93+3079del	ENSP00000395885.1:n.*93+3076_*93+3079del
NM_000268.3:c.1575-40_1575-37del , LRG_511t1:c.1575-40_1575-37del	NP_000259.1:n.1575-40_1575-37del
NM_016418.5:c.1575-40_1575-37del , LRG_511t2:c.1575-40_1575-37del	NP_057502.2:n.1575-40_1575-37del
NM_181825.2:c.1575-40_1575-37del	NP_861546.1:n.1575-40_1575-37del
NM_181828.2:c.1449-40_1449-37del	NP_861966.1:n.1449-40_1449-37del
NM_181829.2:c.1452-40_1452-37del	NP_861967.1:n.1452-40_1452-37del
NM_181830.2:c.1326-40_1326-37del	NP_861968.1:n.1326-40_1326-37del
NM_181831.2:c.1326-40_1326-37del	NP_861969.1:n.1326-40_1326-37del
NM_181832.2:c.1575-40_1575-37del	NP_861970.1:n.1575-40_1575-37del
NM_181833.2:c.448-13353_448-13350del	NP_861971.1:n.448-13353_448-13350del
NR_156186.1:n.2134-40_2134-37del
XM_017028809.2:c.1461-40_1461-37del	XP_016884298.1:n.1461-40_1461-37del
XM_017028810.1:c.1461-40_1461-37del	XP_016884299.1:n.1461-40_1461-37del
NM_000268.4:c.1575-40_1575-37del MANE Select	NP_000259.1:n.1575-40_1575-37del
NM_181825.3:c.1575-40_1575-37del	NP_861546.1:n.1575-40_1575-37del
NM_181828.3:c.1449-40_1449-37del	NP_861966.1:n.1449-40_1449-37del
NM_181829.3:c.1452-40_1452-37del	NP_861967.1:n.1452-40_1452-37del
NM_181830.3:c.1326-40_1326-37del	NP_861968.1:n.1326-40_1326-37del
NM_181831.3:c.1326-40_1326-37del	NP_861969.1:n.1326-40_1326-37del
NM_181832.3:c.1575-40_1575-37del	NP_861970.1:n.1575-40_1575-37del
NR_156186.2:n.2057-40_2057-37del
NM_181833.3:c.448-13353_448-13350del	NP_861971.1:n.448-13353_448-13350del