Canonical Allele Identifier: CA16616358

Gene: NF2

Linked Data

• ClinVar Variation Id: 412207
• ClinVar RCV Id: RCV000458184
• dbSNP Id: rs1060503670
• MyVariant Identifiers: chr22:g.30051581A>G (hg19) ; chr22:g.29655592A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29655592A>G , CM000684.2:g.29655592A>G	GRCh38
NC_000022.10:g.30051581A>G , CM000684.1:g.30051581A>G	GRCh37
NC_000022.9:g.28381581A>G	NCBI36
NG_009057.1:g.57037A>G , LRG_511:g.57037A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.517-2A>G	ENSP00000354529.6:n.517-2A>G
ENST00000673312.2:c.*11-2A>G	ENSP00000500186.2:n.*11-2A>G
ENST00000338641.10:c.517-2A>G MANE Select	ENSP00000344666.5:n.517-2A>G
ENST00000361166.9:c.70-2A>G	ENSP00000354529.5:n.70-2A>G
ENST00000672461.1:c.517-2A>G	ENSP00000500919.1:n.517-2A>G
ENST00000672805.1:c.*399-2A>G	ENSP00000500295.1:n.*399-2A>G
ENST00000672896.1:c.517-2A>G	ENSP00000500117.1:n.517-2A>G
ENST00000673312.1:c.536-2A>G	ENSP00000500186.1:n.536-2A>G
ENST00000334961.11:c.268-2A>G	ENSP00000335652.7:n.268-2A>G
ENST00000338641.8:c.517-2A>G	ENSP00000344666.4:n.517-2A>G
ENST00000353887.8:c.268-2A>G	ENSP00000340626.4:n.268-2A>G
ENST00000361166.8:c.517-2A>G	ENSP00000354529.4:n.517-2A>G
ENST00000361452.8:c.394-2A>G	ENSP00000354897.4:n.394-2A>G
ENST00000361676.8:c.391-2A>G	ENSP00000355183.4:n.391-2A>G
ENST00000397789.3:c.517-2A>G	ENSP00000380891.3:n.517-2A>G
ENST00000403435.5:c.517-2A>G	ENSP00000384029.1:n.517-2A>G
ENST00000403999.7:c.517-2A>G	ENSP00000384797.3:n.517-2A>G
ENST00000413209.6:c.447+13307A>G	ENSP00000409921.2:n.447+13307A>G
ENST00000432151.5:c.199-5613A>G	ENSP00000395885.1:n.199-5613A>G
NM_000268.3:c.517-2A>G , LRG_511t1:c.517-2A>G	NP_000259.1:n.517-2A>G
NM_016418.5:c.517-2A>G , LRG_511t2:c.517-2A>G	NP_057502.2:n.517-2A>G
NM_181825.2:c.517-2A>G	NP_861546.1:n.517-2A>G
NM_181828.2:c.391-2A>G	NP_861966.1:n.391-2A>G
NM_181829.2:c.394-2A>G	NP_861967.1:n.394-2A>G
NM_181830.2:c.268-2A>G	NP_861968.1:n.268-2A>G
NM_181831.2:c.268-2A>G	NP_861969.1:n.268-2A>G
NM_181832.2:c.517-2A>G	NP_861970.1:n.517-2A>G
NM_181833.2:c.447+13307A>G	NP_861971.1:n.447+13307A>G
NR_156186.1:n.1076-2A>G
XM_017028809.2:c.403-2A>G	XP_016884298.1:n.403-2A>G
XM_017028810.1:c.403-2A>G	XP_016884299.1:n.403-2A>G
NM_000268.4:c.517-2A>G MANE Select	NP_000259.1:n.517-2A>G
NM_181825.3:c.517-2A>G	NP_861546.1:n.517-2A>G
NM_181828.3:c.391-2A>G	NP_861966.1:n.391-2A>G
NM_181829.3:c.394-2A>G	NP_861967.1:n.394-2A>G
NM_181830.3:c.268-2A>G	NP_861968.1:n.268-2A>G
NM_181831.3:c.268-2A>G	NP_861969.1:n.268-2A>G
NM_181832.3:c.517-2A>G	NP_861970.1:n.517-2A>G
NR_156186.2:n.999-2A>G
NM_181833.3:c.447+13307A>G	NP_861971.1:n.447+13307A>G