Canonical Allele Identifier: CA031457

Gene: NF2

Linked Data

• ClinVar Variation Id: 457900
• ClinVar RCV Id: RCV000541824 ; RCV001011622
• dbSNP Id: rs367829184
• ExAC: 22:30070935 G / A
• gnomAD v2: 22-30070935-G-A
• gnomAD v3: 22-29674946-G-A
• gnomAD v4: 22-29674946-G-A
• MyVariant Identifiers: chr22:g.30070935G>A (hg19) ; chr22:g.29674946G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29674946G>A , CM000684.2:g.29674946G>A	GRCh38
NC_000022.10:g.30070935G>A , CM000684.1:g.30070935G>A	GRCh37
NC_000022.9:g.28400935G>A	NCBI36
NG_009057.1:g.76391G>A , LRG_511:g.76391G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1311+5G>A	ENSP00000354529.6:n.1311+5G>A
ENST00000673312.2:c.*940+5G>A	ENSP00000500186.2:n.*940+5G>A
ENST00000338641.10:c.1446+5G>A MANE Select	ENSP00000344666.5:n.1446+5G>A
ENST00000361166.9:c.864+5G>A	ENSP00000354529.5:n.864+5G>A
ENST00000672461.1:c.1446+5G>A	ENSP00000500919.1:n.1446+5G>A
ENST00000672805.1:c.*1328+5G>A	ENSP00000500295.1:n.*1328+5G>A
ENST00000672896.1:c.1446+5G>A	ENSP00000500117.1:n.1446+5G>A
ENST00000673312.1:c.1465+5G>A	ENSP00000500186.1:n.1465+5G>A
ENST00000334961.11:c.1197+5G>A	ENSP00000335652.7:n.1197+5G>A
ENST00000338641.8:c.1446+5G>A	ENSP00000344666.4:n.1446+5G>A
ENST00000353887.8:c.1197+5G>A	ENSP00000340626.4:n.1197+5G>A
ENST00000361166.8:c.1446+5G>A	ENSP00000354529.4:n.1446+5G>A
ENST00000361452.8:c.1323+5G>A	ENSP00000354897.4:n.1323+5G>A
ENST00000361676.8:c.1320+5G>A	ENSP00000355183.4:n.1320+5G>A
ENST00000397789.3:c.1446+5G>A	ENSP00000380891.3:n.1446+5G>A
ENST00000403435.5:c.1359+5G>A	ENSP00000384029.1:n.1359+5G>A
ENST00000403999.7:c.1446+5G>A	ENSP00000384797.3:n.1446+5G>A
ENST00000413209.6:c.448-19806G>A	ENSP00000409921.2:n.448-19806G>A
ENST00000432151.5:c.628+5G>A	ENSP00000395885.1:n.628+5G>A
NM_000268.3:c.1446+5G>A , LRG_511t1:c.1446+5G>A	NP_000259.1:n.1446+5G>A
NM_016418.5:c.1446+5G>A , LRG_511t2:c.1446+5G>A	NP_057502.2:n.1446+5G>A
NM_181825.2:c.1446+5G>A	NP_861546.1:n.1446+5G>A
NM_181828.2:c.1320+5G>A	NP_861966.1:n.1320+5G>A
NM_181829.2:c.1323+5G>A	NP_861967.1:n.1323+5G>A
NM_181830.2:c.1197+5G>A	NP_861968.1:n.1197+5G>A
NM_181831.2:c.1197+5G>A	NP_861969.1:n.1197+5G>A
NM_181832.2:c.1446+5G>A	NP_861970.1:n.1446+5G>A
NM_181833.2:c.448-19806G>A	NP_861971.1:n.448-19806G>A
NR_156186.1:n.2005+5G>A
XM_017028809.2:c.1332+5G>A	XP_016884298.1:n.1332+5G>A
XM_017028810.1:c.1332+5G>A	XP_016884299.1:n.1332+5G>A
NM_000268.4:c.1446+5G>A MANE Select	NP_000259.1:n.1446+5G>A
NM_181825.3:c.1446+5G>A	NP_861546.1:n.1446+5G>A
NM_181828.3:c.1320+5G>A	NP_861966.1:n.1320+5G>A
NM_181829.3:c.1323+5G>A	NP_861967.1:n.1323+5G>A
NM_181830.3:c.1197+5G>A	NP_861968.1:n.1197+5G>A
NM_181831.3:c.1197+5G>A	NP_861969.1:n.1197+5G>A
NM_181832.3:c.1446+5G>A	NP_861970.1:n.1446+5G>A
NR_156186.2:n.1928+5G>A
NM_181833.3:c.448-19806G>A	NP_861971.1:n.448-19806G>A