Canonical Allele Identifier: CA2656032969

Gene: NF2

Linked Data

• gnomAD v4: 22-29694891-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694891A>G , CM000684.2:g.29694891A>G	GRCh38
NC_000022.10:g.30090880A>G , CM000684.1:g.30090880A>G	GRCh37
NC_000022.9:g.28420880A>G	NCBI36
NG_009057.1:g.96336A>G , LRG_511:g.96336A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*89A>G	ENSP00000354529.6:n.*89A>G
ENST00000673312.2:c.*1371A>G	ENSP00000500186.2:n.*1371A>G
ENST00000338641.10:c.*89A>G MANE Select	ENSP00000344666.5:n.*89A>G
ENST00000361166.9:c.1295A>G	ENSP00000354529.5:n.1295A>G
ENST00000672461.1:c.*149A>G	ENSP00000500919.1:n.*149A>G
ENST00000672805.1:c.*1759A>G	ENSP00000500295.1:n.*1759A>G
ENST00000672896.1:c.*149A>G	ENSP00000500117.1:n.*149A>G
ENST00000673312.1:c.1896A>G	ENSP00000500186.1:n.1896A>G
ENST00000338641.8:c.*89A>G	ENSP00000344666.4:n.*89A>G
ENST00000361452.8:c.*149A>G	ENSP00000354897.4:n.*149A>G
ENST00000413209.6:c.*89A>G	ENSP00000409921.2:n.*89A>G
ENST00000432151.5:c.*233A>G	ENSP00000395885.1:n.*233A>G
NM_000268.3:c.*89A>G , LRG_511t1:c.*89A>G	NP_000259.1:n.*89A>G
NM_016418.5:c.*149A>G , LRG_511t2:c.*149A>G	NP_057502.2:n.*149A>G
NM_181828.2:c.*149A>G	NP_861966.1:n.*149A>G
NM_181829.2:c.*149A>G	NP_861967.1:n.*149A>G
NM_181830.2:c.*149A>G	NP_861968.1:n.*149A>G
NM_181832.2:c.*164A>G	NP_861970.1:n.*164A>G
NM_181833.2:c.*89A>G	NP_861971.1:n.*89A>G
NR_156186.1:n.2436A>G
XM_017028809.2:c.*89A>G	XP_016884298.1:n.*89A>G
XM_017028810.1:c.*149A>G	XP_016884299.1:n.*149A>G
NM_000268.4:c.*89A>G MANE Select	NP_000259.1:n.*89A>G
NM_181828.3:c.*149A>G	NP_861966.1:n.*149A>G
NM_181829.3:c.*149A>G	NP_861967.1:n.*149A>G
NM_181830.3:c.*149A>G	NP_861968.1:n.*149A>G
NM_181832.3:c.*164A>G	NP_861970.1:n.*164A>G
NR_156186.2:n.2359A>G
NM_181833.3:c.*89A>G	NP_861971.1:n.*89A>G