Canonical Allele Identifier: CA411148810

Gene: NF2

Linked Data

• ClinVar Variation Id: 1770382
• ClinVar RCV Id: RCV002387730 ; RCV003464510 ; RCV003774273
• dbSNP Id: rs2066911364
• gnomAD v4: 22-29674836-G-T
• MyVariant Identifiers: chr22:g.30070825G>T (hg19) ; chr22:g.29674836G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29674836G>T , CM000684.2:g.29674836G>T	GRCh38
NC_000022.10:g.30070825G>T , CM000684.1:g.30070825G>T	GRCh37
NC_000022.9:g.28400825G>T	NCBI36
NG_009057.1:g.76281G>T , LRG_511:g.76281G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1206G>T	ENSP00000354529.6:p.Arg402Ser
ENST00000673312.2:c.*835G>T	ENSP00000500186.2:n.*835G>T
ENST00000338641.10:c.1341G>T MANE Select	ENSP00000344666.5:p.Arg447Ser
ENST00000361166.9:c.759G>T	ENSP00000354529.5:p.Arg253Ser
ENST00000672461.1:c.1341G>T	ENSP00000500919.1:p.Arg447Ser
ENST00000672805.1:c.*1223G>T	ENSP00000500295.1:n.*1223G>T
ENST00000672896.1:c.1341G>T	ENSP00000500117.1:p.Arg447Ser
ENST00000673312.1:c.1360G>T	ENSP00000500186.1:n.1360G>T
ENST00000334961.11:c.1092G>T	ENSP00000335652.7:p.Arg364Ser
ENST00000338641.8:c.1341G>T	ENSP00000344666.4:p.Arg447Ser
ENST00000353887.8:c.1092G>T	ENSP00000340626.4:p.Arg364Ser
ENST00000361166.8:c.1341G>T	ENSP00000354529.4:p.Arg447Ser
ENST00000361452.8:c.1218G>T	ENSP00000354897.4:p.Arg406Ser
ENST00000361676.8:c.1215G>T	ENSP00000355183.4:p.Arg405Ser
ENST00000397789.3:c.1341G>T	ENSP00000380891.3:p.Arg447Ser
ENST00000403435.5:c.1254G>T	ENSP00000384029.1:p.Arg418Ser
ENST00000403999.7:c.1341G>T	ENSP00000384797.3:p.Arg447Ser
ENST00000413209.6:c.448-19916G>T	ENSP00000409921.2:n.448-19916G>T
ENST00000432151.5:c.523G>T	ENSP00000395885.1:p.Gly175Cys
NM_000268.3:c.1341G>T , LRG_511t1:c.1341G>T	NP_000259.1:p.Arg447Ser
NM_016418.5:c.1341G>T , LRG_511t2:c.1341G>T	NP_057502.2:p.Arg447Ser
NM_181825.2:c.1341G>T	NP_861546.1:p.Arg447Ser
NM_181828.2:c.1215G>T	NP_861966.1:p.Arg405Ser
NM_181829.2:c.1218G>T	NP_861967.1:p.Arg406Ser
NM_181830.2:c.1092G>T	NP_861968.1:p.Arg364Ser
NM_181831.2:c.1092G>T	NP_861969.1:p.Arg364Ser
NM_181832.2:c.1341G>T	NP_861970.1:p.Arg447Ser
NM_181833.2:c.448-19916G>T	NP_861971.1:n.448-19916G>T
NR_156186.1:n.1900G>T
XM_017028809.2:c.1227G>T	XP_016884298.1:p.Arg409Ser
XM_017028810.1:c.1227G>T	XP_016884299.1:p.Arg409Ser
NM_000268.4:c.1341G>T MANE Select	NP_000259.1:p.Arg447Ser
NM_181825.3:c.1341G>T	NP_861546.1:p.Arg447Ser
NM_181828.3:c.1215G>T	NP_861966.1:p.Arg405Ser
NM_181829.3:c.1218G>T	NP_861967.1:p.Arg406Ser
NM_181830.3:c.1092G>T	NP_861968.1:p.Arg364Ser
NM_181831.3:c.1092G>T	NP_861969.1:p.Arg364Ser
NM_181832.3:c.1341G>T	NP_861970.1:p.Arg447Ser
NR_156186.2:n.1823G>T
NM_181833.3:c.448-19916G>T	NP_861971.1:n.448-19916G>T