Canonical Allele Identifier: CA411149704

Gene: NF2

Linked Data

• MyVariant Identifiers: chr22:g.30074263T>A (hg19) ; chr22:g.29678274T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29678274T>A , CM000684.2:g.29678274T>A	GRCh38
NC_000022.10:g.30074263T>A , CM000684.1:g.30074263T>A	GRCh37
NC_000022.9:g.28404263T>A	NCBI36
NG_009057.1:g.79719T>A , LRG_511:g.79719T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1390T>A	ENSP00000354529.6:p.Phe464Ile
ENST00000673312.2:c.*1019T>A	ENSP00000500186.2:n.*1019T>A
ENST00000338641.10:c.1525T>A MANE Select	ENSP00000344666.5:p.Phe509Ile
ENST00000361166.9:c.943T>A	ENSP00000354529.5:p.Phe315Ile
ENST00000672461.1:c.1525T>A	ENSP00000500919.1:p.Phe509Ile
ENST00000672805.1:c.*1407T>A	ENSP00000500295.1:n.*1407T>A
ENST00000672896.1:c.1525T>A	ENSP00000500117.1:p.Phe509Ile
ENST00000673312.1:c.1544T>A	ENSP00000500186.1:n.1544T>A
ENST00000334961.11:c.1276T>A	ENSP00000335652.7:p.Phe426Ile
ENST00000338641.8:c.1525T>A	ENSP00000344666.4:p.Phe509Ile
ENST00000353887.8:c.1276T>A	ENSP00000340626.4:p.Phe426Ile
ENST00000361166.8:c.1525T>A	ENSP00000354529.4:p.Phe509Ile
ENST00000361452.8:c.1402T>A	ENSP00000354897.4:p.Phe468Ile
ENST00000361676.8:c.1399T>A	ENSP00000355183.4:p.Phe467Ile
ENST00000397789.3:c.1525T>A	ENSP00000380891.3:p.Phe509Ile
ENST00000403435.5:c.1438T>A	ENSP00000384029.1:p.Phe480Ile
ENST00000403999.7:c.1525T>A	ENSP00000384797.3:p.Phe509Ile
ENST00000413209.6:c.448-16478T>A	ENSP00000409921.2:n.448-16478T>A
ENST00000432151.5:c.*44T>A	ENSP00000395885.1:n.*44T>A
NM_000268.3:c.1525T>A , LRG_511t1:c.1525T>A	NP_000259.1:p.Phe509Ile
NM_016418.5:c.1525T>A , LRG_511t2:c.1525T>A	NP_057502.2:p.Phe509Ile
NM_181825.2:c.1525T>A	NP_861546.1:p.Phe509Ile
NM_181828.2:c.1399T>A	NP_861966.1:p.Phe467Ile
NM_181829.2:c.1402T>A	NP_861967.1:p.Phe468Ile
NM_181830.2:c.1276T>A	NP_861968.1:p.Phe426Ile
NM_181831.2:c.1276T>A	NP_861969.1:p.Phe426Ile
NM_181832.2:c.1525T>A	NP_861970.1:p.Phe509Ile
NM_181833.2:c.448-16478T>A	NP_861971.1:n.448-16478T>A
NR_156186.1:n.2084T>A
XM_017028809.2:c.1411T>A	XP_016884298.1:p.Phe471Ile
XM_017028810.1:c.1411T>A	XP_016884299.1:p.Phe471Ile
NM_000268.4:c.1525T>A MANE Select	NP_000259.1:p.Phe509Ile
NM_181825.3:c.1525T>A	NP_861546.1:p.Phe509Ile
NM_181828.3:c.1399T>A	NP_861966.1:p.Phe467Ile
NM_181829.3:c.1402T>A	NP_861967.1:p.Phe468Ile
NM_181830.3:c.1276T>A	NP_861968.1:p.Phe426Ile
NM_181831.3:c.1276T>A	NP_861969.1:p.Phe426Ile
NM_181832.3:c.1525T>A	NP_861970.1:p.Phe509Ile
NR_156186.2:n.2007T>A
NM_181833.3:c.448-16478T>A	NP_861971.1:n.448-16478T>A