Canonical Allele Identifier: CA411148839

Gene: NF2

Linked Data

• ClinVar Variation Id: 1770671
• ClinVar RCV Id: RCV002383328
• dbSNP Id: rs2066911994
• MyVariant Identifiers: chr22:g.30070838G>A (hg19) ; chr22:g.29674849G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29674849G>A , CM000684.2:g.29674849G>A	GRCh38
NC_000022.10:g.30070838G>A , CM000684.1:g.30070838G>A	GRCh37
NC_000022.9:g.28400838G>A	NCBI36
NG_009057.1:g.76294G>A , LRG_511:g.76294G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1219G>A	ENSP00000354529.6:p.Asp407Asn
ENST00000673312.2:c.*848G>A	ENSP00000500186.2:n.*848G>A
ENST00000338641.10:c.1354G>A MANE Select	ENSP00000344666.5:p.Asp452Asn
ENST00000361166.9:c.772G>A	ENSP00000354529.5:p.Asp258Asn
ENST00000672461.1:c.1354G>A	ENSP00000500919.1:p.Asp452Asn
ENST00000672805.1:c.*1236G>A	ENSP00000500295.1:n.*1236G>A
ENST00000672896.1:c.1354G>A	ENSP00000500117.1:p.Asp452Asn
ENST00000673312.1:c.1373G>A	ENSP00000500186.1:n.1373G>A
ENST00000334961.11:c.1105G>A	ENSP00000335652.7:p.Asp369Asn
ENST00000338641.8:c.1354G>A	ENSP00000344666.4:p.Asp452Asn
ENST00000353887.8:c.1105G>A	ENSP00000340626.4:p.Asp369Asn
ENST00000361166.8:c.1354G>A	ENSP00000354529.4:p.Asp452Asn
ENST00000361452.8:c.1231G>A	ENSP00000354897.4:p.Asp411Asn
ENST00000361676.8:c.1228G>A	ENSP00000355183.4:p.Asp410Asn
ENST00000397789.3:c.1354G>A	ENSP00000380891.3:p.Asp452Asn
ENST00000403435.5:c.1267G>A	ENSP00000384029.1:p.Asp423Asn
ENST00000403999.7:c.1354G>A	ENSP00000384797.3:p.Asp452Asn
ENST00000413209.6:c.448-19903G>A	ENSP00000409921.2:n.448-19903G>A
ENST00000432151.5:c.536G>A	ENSP00000395885.1:p.Arg179Lys
NM_000268.3:c.1354G>A , LRG_511t1:c.1354G>A	NP_000259.1:p.Asp452Asn
NM_016418.5:c.1354G>A , LRG_511t2:c.1354G>A	NP_057502.2:p.Asp452Asn
NM_181825.2:c.1354G>A	NP_861546.1:p.Asp452Asn
NM_181828.2:c.1228G>A	NP_861966.1:p.Asp410Asn
NM_181829.2:c.1231G>A	NP_861967.1:p.Asp411Asn
NM_181830.2:c.1105G>A	NP_861968.1:p.Asp369Asn
NM_181831.2:c.1105G>A	NP_861969.1:p.Asp369Asn
NM_181832.2:c.1354G>A	NP_861970.1:p.Asp452Asn
NM_181833.2:c.448-19903G>A	NP_861971.1:n.448-19903G>A
NR_156186.1:n.1913G>A
XM_017028809.2:c.1240G>A	XP_016884298.1:p.Asp414Asn
XM_017028810.1:c.1240G>A	XP_016884299.1:p.Asp414Asn
NM_000268.4:c.1354G>A MANE Select	NP_000259.1:p.Asp452Asn
NM_181825.3:c.1354G>A	NP_861546.1:p.Asp452Asn
NM_181828.3:c.1228G>A	NP_861966.1:p.Asp410Asn
NM_181829.3:c.1231G>A	NP_861967.1:p.Asp411Asn
NM_181830.3:c.1105G>A	NP_861968.1:p.Asp369Asn
NM_181831.3:c.1105G>A	NP_861969.1:p.Asp369Asn
NM_181832.3:c.1354G>A	NP_861970.1:p.Asp452Asn
NR_156186.2:n.1836G>A
NM_181833.3:c.448-19903G>A	NP_861971.1:n.448-19903G>A