Canonical Allele Identifier: CA411148811

Gene: NF2

Linked Data

• ClinVar Variation Id: 965877
• ClinVar RCV Id: RCV001240426
• dbSNP Id: rs2066911470
• gnomAD v4: 22-29674837-G-A
• MyVariant Identifiers: chr22:g.30070826G>A (hg19) ; chr22:g.29674837G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29674837G>A , CM000684.2:g.29674837G>A	GRCh38
NC_000022.10:g.30070826G>A , CM000684.1:g.30070826G>A	GRCh37
NC_000022.9:g.28400826G>A	NCBI36
NG_009057.1:g.76282G>A , LRG_511:g.76282G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.1207G>A	ENSP00000354529.6:p.Ala403Thr
ENST00000673312.2:c.*836G>A	ENSP00000500186.2:n.*836G>A
ENST00000338641.10:c.1342G>A MANE Select	ENSP00000344666.5:p.Ala448Thr
ENST00000361166.9:c.760G>A	ENSP00000354529.5:p.Ala254Thr
ENST00000672461.1:c.1342G>A	ENSP00000500919.1:p.Ala448Thr
ENST00000672805.1:c.*1224G>A	ENSP00000500295.1:n.*1224G>A
ENST00000672896.1:c.1342G>A	ENSP00000500117.1:p.Ala448Thr
ENST00000673312.1:c.1361G>A	ENSP00000500186.1:n.1361G>A
ENST00000334961.11:c.1093G>A	ENSP00000335652.7:p.Ala365Thr
ENST00000338641.8:c.1342G>A	ENSP00000344666.4:p.Ala448Thr
ENST00000353887.8:c.1093G>A	ENSP00000340626.4:p.Ala365Thr
ENST00000361166.8:c.1342G>A	ENSP00000354529.4:p.Ala448Thr
ENST00000361452.8:c.1219G>A	ENSP00000354897.4:p.Ala407Thr
ENST00000361676.8:c.1216G>A	ENSP00000355183.4:p.Ala406Thr
ENST00000397789.3:c.1342G>A	ENSP00000380891.3:p.Ala448Thr
ENST00000403435.5:c.1255G>A	ENSP00000384029.1:p.Ala419Thr
ENST00000403999.7:c.1342G>A	ENSP00000384797.3:p.Ala448Thr
ENST00000413209.6:c.448-19915G>A	ENSP00000409921.2:n.448-19915G>A
ENST00000432151.5:c.524G>A	ENSP00000395885.1:p.Gly175Asp
NM_000268.3:c.1342G>A , LRG_511t1:c.1342G>A	NP_000259.1:p.Ala448Thr
NM_016418.5:c.1342G>A , LRG_511t2:c.1342G>A	NP_057502.2:p.Ala448Thr
NM_181825.2:c.1342G>A	NP_861546.1:p.Ala448Thr
NM_181828.2:c.1216G>A	NP_861966.1:p.Ala406Thr
NM_181829.2:c.1219G>A	NP_861967.1:p.Ala407Thr
NM_181830.2:c.1093G>A	NP_861968.1:p.Ala365Thr
NM_181831.2:c.1093G>A	NP_861969.1:p.Ala365Thr
NM_181832.2:c.1342G>A	NP_861970.1:p.Ala448Thr
NM_181833.2:c.448-19915G>A	NP_861971.1:n.448-19915G>A
NR_156186.1:n.1901G>A
XM_017028809.2:c.1228G>A	XP_016884298.1:p.Ala410Thr
XM_017028810.1:c.1228G>A	XP_016884299.1:p.Ala410Thr
NM_000268.4:c.1342G>A MANE Select	NP_000259.1:p.Ala448Thr
NM_181825.3:c.1342G>A	NP_861546.1:p.Ala448Thr
NM_181828.3:c.1216G>A	NP_861966.1:p.Ala406Thr
NM_181829.3:c.1219G>A	NP_861967.1:p.Ala407Thr
NM_181830.3:c.1093G>A	NP_861968.1:p.Ala365Thr
NM_181831.3:c.1093G>A	NP_861969.1:p.Ala365Thr
NM_181832.3:c.1342G>A	NP_861970.1:p.Ala448Thr
NR_156186.2:n.1824G>A
NM_181833.3:c.448-19915G>A	NP_861971.1:n.448-19915G>A