Canonical Allele Identifier: CA514183147

Gene: NF2

Linked Data

• dbSNP Id: rs2147008724
• MyVariant Identifiers: chr22:g.30057235G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29661246G>C , CM000684.2:g.29661246G>C	GRCh38
NC_000022.10:g.30057235G>C , CM000684.1:g.30057235G>C	GRCh37
NC_000022.9:g.28387235G>C	NCBI36
NG_009057.1:g.62691G>C , LRG_511:g.62691G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.675+2982G>C	ENSP00000354529.6:n.675+2982G>C
ENST00000673312.2:c.*211G>C	ENSP00000500186.2:n.*211G>C
ENST00000338641.10:c.717G>C MANE Select	ENSP00000344666.5:p.Leu239=
ENST00000361166.9:c.228+2982G>C	ENSP00000354529.5:n.228+2982G>C
ENST00000672461.1:c.717G>C	ENSP00000500919.1:p.Leu239=
ENST00000672805.1:c.*599G>C	ENSP00000500295.1:n.*599G>C
ENST00000672896.1:c.717G>C	ENSP00000500117.1:p.Leu239=
ENST00000673312.1:c.736G>C	ENSP00000500186.1:n.736G>C
ENST00000334961.11:c.468G>C	ENSP00000335652.7:p.Leu156=
ENST00000338641.8:c.717G>C	ENSP00000344666.4:p.Leu239=
ENST00000353887.8:c.468G>C	ENSP00000340626.4:p.Leu156=
ENST00000361166.8:c.717G>C	ENSP00000354529.4:p.Leu239=
ENST00000361452.8:c.594G>C	ENSP00000354897.4:p.Leu198=
ENST00000361676.8:c.591G>C	ENSP00000355183.4:p.Leu197=
ENST00000397789.3:c.717G>C	ENSP00000380891.3:p.Leu239=
ENST00000403435.5:c.717G>C	ENSP00000384029.1:p.Leu239=
ENST00000403999.7:c.717G>C	ENSP00000384797.3:p.Leu239=
ENST00000413209.6:c.447+18961G>C	ENSP00000409921.2:n.447+18961G>C
ENST00000432151.5:c.240G>C	ENSP00000395885.1:p.Leu80=
NM_000268.3:c.717G>C , LRG_511t1:c.717G>C	NP_000259.1:p.Leu239=
NM_016418.5:c.717G>C , LRG_511t2:c.717G>C	NP_057502.2:p.Leu239=
NM_181825.2:c.717G>C	NP_861546.1:p.Leu239=
NM_181828.2:c.591G>C	NP_861966.1:p.Leu197=
NM_181829.2:c.594G>C	NP_861967.1:p.Leu198=
NM_181830.2:c.468G>C	NP_861968.1:p.Leu156=
NM_181831.2:c.468G>C	NP_861969.1:p.Leu156=
NM_181832.2:c.717G>C	NP_861970.1:p.Leu239=
NM_181833.2:c.447+18961G>C	NP_861971.1:n.447+18961G>C
NR_156186.1:n.1276G>C
XM_017028809.2:c.603G>C	XP_016884298.1:p.Leu201=
XM_017028810.1:c.603G>C	XP_016884299.1:p.Leu201=
NM_000268.4:c.717G>C MANE Select	NP_000259.1:p.Leu239=
NM_181825.3:c.717G>C	NP_861546.1:p.Leu239=
NM_181828.3:c.591G>C	NP_861966.1:p.Leu197=
NM_181829.3:c.594G>C	NP_861967.1:p.Leu198=
NM_181830.3:c.468G>C	NP_861968.1:p.Leu156=
NM_181831.3:c.468G>C	NP_861969.1:p.Leu156=
NM_181832.3:c.717G>C	NP_861970.1:p.Leu239=
NR_156186.2:n.1199G>C
NM_181833.3:c.447+18961G>C	NP_861971.1:n.447+18961G>C