Canonical Allele Identifier: CA2656033011

Gene: NF2

Linked Data

• gnomAD v4: 22-29694910-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694913del , CM000684.2:g.29694913del	GRCh38
NC_000022.10:g.30090902del , CM000684.1:g.30090902del	GRCh37
NC_000022.9:g.28420902del	NCBI36
NG_009057.1:g.96358del , LRG_511:g.96358del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*111del	ENSP00000354529.6:n.*111del
ENST00000673312.2:c.*1393del	ENSP00000500186.2:n.*1393del
ENST00000338641.10:c.*111del MANE Select	ENSP00000344666.5:n.*111del
ENST00000361166.9:c.1317del	ENSP00000354529.5:n.1317del
ENST00000672461.1:c.*171del	ENSP00000500919.1:n.*171del
ENST00000672805.1:c.*1781del	ENSP00000500295.1:n.*1781del
ENST00000672896.1:c.*171del	ENSP00000500117.1:n.*171del
ENST00000673312.1:c.1918del	ENSP00000500186.1:n.1918del
ENST00000338641.8:c.*111del	ENSP00000344666.4:n.*111del
ENST00000361452.8:c.*171del	ENSP00000354897.4:n.*171del
ENST00000413209.6:c.*111del	ENSP00000409921.2:n.*111del
ENST00000432151.5:c.*255del	ENSP00000395885.1:n.*255del
NM_000268.3:c.*111del , LRG_511t1:c.*111del	NP_000259.1:n.*111del
NM_016418.5:c.*171del , LRG_511t2:c.*171del	NP_057502.2:n.*171del
NM_181828.2:c.*171del	NP_861966.1:n.*171del
NM_181829.2:c.*171del	NP_861967.1:n.*171del
NM_181830.2:c.*171del	NP_861968.1:n.*171del
NM_181832.2:c.*186del	NP_861970.1:n.*186del
NM_181833.2:c.*111del	NP_861971.1:n.*111del
NR_156186.1:n.2458del
XM_017028809.2:c.*111del	XP_016884298.1:n.*111del
XM_017028810.1:c.*171del	XP_016884299.1:n.*171del
NM_000268.4:c.*111del MANE Select	NP_000259.1:n.*111del
NM_181828.3:c.*171del	NP_861966.1:n.*171del
NM_181829.3:c.*171del	NP_861967.1:n.*171del
NM_181830.3:c.*171del	NP_861968.1:n.*171del
NM_181832.3:c.*186del	NP_861970.1:n.*186del
NR_156186.2:n.2381del
NM_181833.3:c.*111del	NP_861971.1:n.*111del