Canonical Allele Identifier: CA411148398

Gene: NF2

Linked Data

• ClinVar Variation Id: 2677244
• ClinVar RCV Id: RCV003463176
• MyVariant Identifiers: chr22:g.30069406G>C (hg19) ; chr22:g.29673417G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29673417G>C , CM000684.2:g.29673417G>C	GRCh38
NC_000022.10:g.30069406G>C , CM000684.1:g.30069406G>C	GRCh37
NC_000022.9:g.28399406G>C	NCBI36
NG_009057.1:g.74862G>C , LRG_511:g.74862G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1136G>C	ENSP00000354529.6:p.Arg379Pro
ENST00000673312.2:c.*765G>C	ENSP00000500186.2:n.*765G>C
ENST00000338641.10:c.1271G>C MANE Select	ENSP00000344666.5:p.Arg424Pro
ENST00000361166.9:c.689G>C	ENSP00000354529.5:p.Arg230Pro
ENST00000672461.1:c.1271G>C	ENSP00000500919.1:p.Arg424Pro
ENST00000672805.1:c.*1153G>C	ENSP00000500295.1:n.*1153G>C
ENST00000672896.1:c.1271G>C	ENSP00000500117.1:p.Arg424Pro
ENST00000673312.1:c.1290G>C	ENSP00000500186.1:n.1290G>C
ENST00000334961.11:c.1022G>C	ENSP00000335652.7:p.Arg341Pro
ENST00000338641.8:c.1271G>C	ENSP00000344666.4:p.Arg424Pro
ENST00000353887.8:c.1022G>C	ENSP00000340626.4:p.Arg341Pro
ENST00000361166.8:c.1271G>C	ENSP00000354529.4:p.Arg424Pro
ENST00000361452.8:c.1148G>C	ENSP00000354897.4:p.Arg383Pro
ENST00000361676.8:c.1145G>C	ENSP00000355183.4:p.Arg382Pro
ENST00000397789.3:c.1271G>C	ENSP00000380891.3:p.Arg424Pro
ENST00000403435.5:c.1184G>C	ENSP00000384029.1:p.Arg395Pro
ENST00000403999.7:c.1271G>C	ENSP00000384797.3:p.Arg424Pro
ENST00000413209.6:c.448-21335G>C	ENSP00000409921.2:n.448-21335G>C
ENST00000432151.5:c.523-1419G>C	ENSP00000395885.1:n.523-1419G>C
NM_000268.3:c.1271G>C , LRG_511t1:c.1271G>C	NP_000259.1:p.Arg424Pro
NM_016418.5:c.1271G>C , LRG_511t2:c.1271G>C	NP_057502.2:p.Arg424Pro
NM_181825.2:c.1271G>C	NP_861546.1:p.Arg424Pro
NM_181828.2:c.1145G>C	NP_861966.1:p.Arg382Pro
NM_181829.2:c.1148G>C	NP_861967.1:p.Arg383Pro
NM_181830.2:c.1022G>C	NP_861968.1:p.Arg341Pro
NM_181831.2:c.1022G>C	NP_861969.1:p.Arg341Pro
NM_181832.2:c.1271G>C	NP_861970.1:p.Arg424Pro
NM_181833.2:c.448-21335G>C	NP_861971.1:n.448-21335G>C
NR_156186.1:n.1830G>C
XM_017028809.2:c.1157G>C	XP_016884298.1:p.Arg386Pro
XM_017028810.1:c.1157G>C	XP_016884299.1:p.Arg386Pro
NM_000268.4:c.1271G>C MANE Select	NP_000259.1:p.Arg424Pro
NM_181825.3:c.1271G>C	NP_861546.1:p.Arg424Pro
NM_181828.3:c.1145G>C	NP_861966.1:p.Arg382Pro
NM_181829.3:c.1148G>C	NP_861967.1:p.Arg383Pro
NM_181830.3:c.1022G>C	NP_861968.1:p.Arg341Pro
NM_181831.3:c.1022G>C	NP_861969.1:p.Arg341Pro
NM_181832.3:c.1271G>C	NP_861970.1:p.Arg424Pro
NR_156186.2:n.1753G>C
NM_181833.3:c.448-21335G>C	NP_861971.1:n.448-21335G>C