Canonical Allele Identifier: CA2656031915

Gene: NF2

Linked Data

• gnomAD v4: 22-29673214-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29673217del , CM000684.2:g.29673217del	GRCh38
NC_000022.10:g.30069206del , CM000684.1:g.30069206del	GRCh37
NC_000022.9:g.28399206del	NCBI36
NG_009057.1:g.74662del , LRG_511:g.74662del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.988-52del	ENSP00000354529.6:n.988-52del
ENST00000673312.2:c.*617-52del	ENSP00000500186.2:n.*617-52del
ENST00000338641.10:c.1123-52del MANE Select	ENSP00000344666.5:n.1123-52del
ENST00000361166.9:c.541-52del	ENSP00000354529.5:n.541-52del
ENST00000672461.1:c.1123-52del	ENSP00000500919.1:n.1123-52del
ENST00000672805.1:c.*1005-52del	ENSP00000500295.1:n.*1005-52del
ENST00000672896.1:c.1123-52del	ENSP00000500117.1:n.1123-52del
ENST00000673312.1:c.1142-52del	ENSP00000500186.1:n.1142-52del
ENST00000334961.11:c.874-52del	ENSP00000335652.7:n.874-52del
ENST00000338641.8:c.1123-52del	ENSP00000344666.4:n.1123-52del
ENST00000353887.8:c.874-52del	ENSP00000340626.4:n.874-52del
ENST00000361166.8:c.1123-52del	ENSP00000354529.4:n.1123-52del
ENST00000361452.8:c.1000-52del	ENSP00000354897.4:n.1000-52del
ENST00000361676.8:c.997-52del	ENSP00000355183.4:n.997-52del
ENST00000397789.3:c.1123-52del	ENSP00000380891.3:n.1123-52del
ENST00000403435.5:c.1036-52del	ENSP00000384029.1:n.1036-52del
ENST00000403999.7:c.1123-52del	ENSP00000384797.3:n.1123-52del
ENST00000413209.6:c.448-21535del	ENSP00000409921.2:n.448-21535del
ENST00000432151.5:c.523-1619del	ENSP00000395885.1:n.523-1619del
NM_000268.3:c.1123-52del , LRG_511t1:c.1123-52del	NP_000259.1:n.1123-52del
NM_016418.5:c.1123-52del , LRG_511t2:c.1123-52del	NP_057502.2:n.1123-52del
NM_181825.2:c.1123-52del	NP_861546.1:n.1123-52del
NM_181828.2:c.997-52del	NP_861966.1:n.997-52del
NM_181829.2:c.1000-52del	NP_861967.1:n.1000-52del
NM_181830.2:c.874-52del	NP_861968.1:n.874-52del
NM_181831.2:c.874-52del	NP_861969.1:n.874-52del
NM_181832.2:c.1123-52del	NP_861970.1:n.1123-52del
NM_181833.2:c.448-21535del	NP_861971.1:n.448-21535del
NR_156186.1:n.1682-52del
XM_017028809.2:c.1009-52del	XP_016884298.1:n.1009-52del
XM_017028810.1:c.1009-52del	XP_016884299.1:n.1009-52del
NM_000268.4:c.1123-52del MANE Select	NP_000259.1:n.1123-52del
NM_181825.3:c.1123-52del	NP_861546.1:n.1123-52del
NM_181828.3:c.997-52del	NP_861966.1:n.997-52del
NM_181829.3:c.1000-52del	NP_861967.1:n.1000-52del
NM_181830.3:c.874-52del	NP_861968.1:n.874-52del
NM_181831.3:c.874-52del	NP_861969.1:n.874-52del
NM_181832.3:c.1123-52del	NP_861970.1:n.1123-52del
NR_156186.2:n.1605-52del
NM_181833.3:c.448-21535del	NP_861971.1:n.448-21535del