Canonical Allele Identifier: CA2656033026

Gene: NF2

Linked Data

• gnomAD v4: 22-29694920-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694920A>G , CM000684.2:g.29694920A>G	GRCh38
NC_000022.10:g.30090909A>G , CM000684.1:g.30090909A>G	GRCh37
NC_000022.9:g.28420909A>G	NCBI36
NG_009057.1:g.96365A>G , LRG_511:g.96365A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*118A>G	ENSP00000354529.6:n.*118A>G
ENST00000673312.2:c.*1400A>G	ENSP00000500186.2:n.*1400A>G
ENST00000338641.10:c.*118A>G MANE Select	ENSP00000344666.5:n.*118A>G
ENST00000361166.9:c.1324A>G	ENSP00000354529.5:n.1324A>G
ENST00000672461.1:c.*178A>G	ENSP00000500919.1:n.*178A>G
ENST00000672805.1:c.*1788A>G	ENSP00000500295.1:n.*1788A>G
ENST00000672896.1:c.*178A>G	ENSP00000500117.1:n.*178A>G
ENST00000673312.1:c.1925A>G	ENSP00000500186.1:n.1925A>G
ENST00000338641.8:c.*118A>G	ENSP00000344666.4:n.*118A>G
ENST00000361452.8:c.*178A>G	ENSP00000354897.4:n.*178A>G
ENST00000413209.6:c.*118A>G	ENSP00000409921.2:n.*118A>G
ENST00000432151.5:c.*262A>G	ENSP00000395885.1:n.*262A>G
NM_000268.3:c.*118A>G , LRG_511t1:c.*118A>G	NP_000259.1:n.*118A>G
NM_016418.5:c.*178A>G , LRG_511t2:c.*178A>G	NP_057502.2:n.*178A>G
NM_181828.2:c.*178A>G	NP_861966.1:n.*178A>G
NM_181829.2:c.*178A>G	NP_861967.1:n.*178A>G
NM_181830.2:c.*178A>G	NP_861968.1:n.*178A>G
NM_181832.2:c.*193A>G	NP_861970.1:n.*193A>G
NM_181833.2:c.*118A>G	NP_861971.1:n.*118A>G
NR_156186.1:n.2465A>G
XM_017028809.2:c.*118A>G	XP_016884298.1:n.*118A>G
XM_017028810.1:c.*178A>G	XP_016884299.1:n.*178A>G
NM_000268.4:c.*118A>G MANE Select	NP_000259.1:n.*118A>G
NM_181828.3:c.*178A>G	NP_861966.1:n.*178A>G
NM_181829.3:c.*178A>G	NP_861967.1:n.*178A>G
NM_181830.3:c.*178A>G	NP_861968.1:n.*178A>G
NM_181832.3:c.*193A>G	NP_861970.1:n.*193A>G
NR_156186.2:n.2388A>G
NM_181833.3:c.*118A>G	NP_861971.1:n.*118A>G