Canonical Allele Identifier: CA411144173

Gene: NF2

Linked Data

• dbSNP Id: rs2147011157
• gnomAD v4: 22-29661329-G-C
• MyVariant Identifiers: chr22:g.30057318G>C (hg19) ; chr22:g.29661329G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29661329G>C , CM000684.2:g.29661329G>C	GRCh38
NC_000022.10:g.30057318G>C , CM000684.1:g.30057318G>C	GRCh37
NC_000022.9:g.28387318G>C	NCBI36
NG_009057.1:g.62774G>C , LRG_511:g.62774G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.675+3065G>C	ENSP00000354529.6:n.675+3065G>C
ENST00000673312.2:c.*294G>C	ENSP00000500186.2:n.*294G>C
ENST00000338641.10:c.800G>C MANE Select	ENSP00000344666.5:p.Ser267Thr
ENST00000361166.9:c.228+3065G>C	ENSP00000354529.5:n.228+3065G>C
ENST00000672461.1:c.800G>C	ENSP00000500919.1:p.Ser267Thr
ENST00000672805.1:c.*682G>C	ENSP00000500295.1:n.*682G>C
ENST00000672896.1:c.800G>C	ENSP00000500117.1:p.Ser267Thr
ENST00000673312.1:c.819G>C	ENSP00000500186.1:n.819G>C
ENST00000334961.11:c.551G>C	ENSP00000335652.7:p.Ser184Thr
ENST00000338641.8:c.800G>C	ENSP00000344666.4:p.Ser267Thr
ENST00000353887.8:c.551G>C	ENSP00000340626.4:p.Ser184Thr
ENST00000361166.8:c.800G>C	ENSP00000354529.4:p.Ser267Thr
ENST00000361452.8:c.677G>C	ENSP00000354897.4:p.Ser226Thr
ENST00000361676.8:c.674G>C	ENSP00000355183.4:p.Ser225Thr
ENST00000397789.3:c.800G>C	ENSP00000380891.3:p.Ser267Thr
ENST00000403435.5:c.800G>C	ENSP00000384029.1:p.Ser267Thr
ENST00000403999.7:c.800G>C	ENSP00000384797.3:p.Ser267Thr
ENST00000413209.6:c.447+19044G>C	ENSP00000409921.2:n.447+19044G>C
ENST00000432151.5:c.323G>C	ENSP00000395885.1:p.Ser108Thr
NM_000268.3:c.800G>C , LRG_511t1:c.800G>C	NP_000259.1:p.Ser267Thr
NM_016418.5:c.800G>C , LRG_511t2:c.800G>C	NP_057502.2:p.Ser267Thr
NM_181825.2:c.800G>C	NP_861546.1:p.Ser267Thr
NM_181828.2:c.674G>C	NP_861966.1:p.Ser225Thr
NM_181829.2:c.677G>C	NP_861967.1:p.Ser226Thr
NM_181830.2:c.551G>C	NP_861968.1:p.Ser184Thr
NM_181831.2:c.551G>C	NP_861969.1:p.Ser184Thr
NM_181832.2:c.800G>C	NP_861970.1:p.Ser267Thr
NM_181833.2:c.447+19044G>C	NP_861971.1:n.447+19044G>C
NR_156186.1:n.1359G>C
XM_017028809.2:c.686G>C	XP_016884298.1:p.Ser229Thr
XM_017028810.1:c.686G>C	XP_016884299.1:p.Ser229Thr
NM_000268.4:c.800G>C MANE Select	NP_000259.1:p.Ser267Thr
NM_181825.3:c.800G>C	NP_861546.1:p.Ser267Thr
NM_181828.3:c.674G>C	NP_861966.1:p.Ser225Thr
NM_181829.3:c.677G>C	NP_861967.1:p.Ser226Thr
NM_181830.3:c.551G>C	NP_861968.1:p.Ser184Thr
NM_181831.3:c.551G>C	NP_861969.1:p.Ser184Thr
NM_181832.3:c.800G>C	NP_861970.1:p.Ser267Thr
NR_156186.2:n.1282G>C
NM_181833.3:c.447+19044G>C	NP_861971.1:n.447+19044G>C