Canonical Allele Identifier: CA411150432
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1442646
ClinVar RCV Id: RCV001960321
dbSNP Id: rs2147123415

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29681572G>A , CM000684.2:g.29681572G>A GRCh38
NC_000022.10:g.30077561G>A , CM000684.1:g.30077561G>A GRCh37
NC_000022.9:g.28407561G>A NCBI36
NG_009057.1:g.83017G>A , LRG_511:g.83017G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361166.10:c.1573G>A ENSP00000354529.6:p.Gly525Ser
ENST00000673312.2:c.*1202G>A ENSP00000500186.2:n.*1202G>A
ENST00000338641.10:c.1708G>A MANE Select ENSP00000344666.5:p.Gly570Ser
ENST00000361166.9:c.1126G>A ENSP00000354529.5:p.Gly376Ser
ENST00000672461.1:c.1708G>A ENSP00000500919.1:p.Gly570Ser
ENST00000672805.1:c.*1590G>A ENSP00000500295.1:n.*1590G>A
ENST00000672896.1:c.1708G>A ENSP00000500117.1:p.Gly570Ser
ENST00000673312.1:c.1727G>A ENSP00000500186.1:n.1727G>A
ENST00000334961.11:c.1459G>A ENSP00000335652.7:p.Gly487Ser
ENST00000338641.8:c.1708G>A ENSP00000344666.4:p.Gly570Ser
ENST00000353887.8:c.1459G>A ENSP00000340626.4:p.Gly487Ser
ENST00000361166.8:c.1708G>A ENSP00000354529.4:p.Gly570Ser
ENST00000361452.8:c.1585G>A ENSP00000354897.4:p.Gly529Ser
ENST00000361676.8:c.1582G>A ENSP00000355183.4:p.Gly528Ser
ENST00000397789.3:c.1708G>A ENSP00000380891.3:p.Gly570Ser
ENST00000403435.5:c.1621G>A ENSP00000384029.1:p.Gly541Ser
ENST00000403999.7:c.1708G>A ENSP00000384797.3:p.Gly570Ser
ENST00000413209.6:c.448-13180G>A ENSP00000409921.2:n.448-13180G>A
ENST00000432151.5:c.*93+3249G>A ENSP00000395885.1:n.*93+3249G>A
NM_000268.3:c.1708G>A , LRG_511t1:c.1708G>A NP_000259.1:p.Gly570Ser
NM_016418.5:c.1708G>A , LRG_511t2:c.1708G>A NP_057502.2:p.Gly570Ser
NM_181825.2:c.1708G>A NP_861546.1:p.Gly570Ser
NM_181828.2:c.1582G>A NP_861966.1:p.Gly528Ser
NM_181829.2:c.1585G>A NP_861967.1:p.Gly529Ser
NM_181830.2:c.1459G>A NP_861968.1:p.Gly487Ser
NM_181831.2:c.1459G>A NP_861969.1:p.Gly487Ser
NM_181832.2:c.1708G>A NP_861970.1:p.Gly570Ser
NM_181833.2:c.448-13180G>A NP_861971.1:n.448-13180G>A
NR_156186.1:n.2267G>A
XM_017028809.2:c.1594G>A XP_016884298.1:p.Gly532Ser
XM_017028810.1:c.1594G>A XP_016884299.1:p.Gly532Ser
NM_000268.4:c.1708G>A MANE Select NP_000259.1:p.Gly570Ser
NM_181825.3:c.1708G>A NP_861546.1:p.Gly570Ser
NM_181828.3:c.1582G>A NP_861966.1:p.Gly528Ser
NM_181829.3:c.1585G>A NP_861967.1:p.Gly529Ser
NM_181830.3:c.1459G>A NP_861968.1:p.Gly487Ser
NM_181831.3:c.1459G>A NP_861969.1:p.Gly487Ser
NM_181832.3:c.1708G>A NP_861970.1:p.Gly570Ser
NR_156186.2:n.2190G>A
NM_181833.3:c.448-13180G>A NP_861971.1:n.448-13180G>A