Canonical Allele Identifier: CA10650982
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 341061
ClinVar RCV Id: RCV000285748
dbSNP Id: rs886057334

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29603715C>A , CM000684.2:g.29603715C>A GRCh38
NC_000022.10:g.29999704C>A , CM000684.1:g.29999704C>A GRCh37
NC_000022.9:g.28329704C>A NCBI36
NG_009057.1:g.5160C>A , LRG_511:g.5160C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361166.10:c.-284C>A ENSP00000354529.6:n.-284C>A
ENST00000673312.2:c.-284C>A ENSP00000500186.2:n.-284C>A
ENST00000338641.10:c.-284C>A MANE Select ENSP00000344666.5:n.-284C>A
ENST00000672461.1:c.-284C>A ENSP00000500919.1:n.-284C>A
ENST00000672805.1:c.-284C>A ENSP00000500295.1:n.-284C>A
ENST00000672896.1:c.-284C>A ENSP00000500117.1:n.-284C>A
ENST00000338641.8:c.-284C>A ENSP00000344666.4:n.-284C>A
ENST00000361452.8:c.-284C>A ENSP00000354897.4:n.-284C>A
ENST00000403435.5:c.-284C>A ENSP00000384029.1:n.-284C>A
ENST00000403999.7:c.-284C>A ENSP00000384797.3:n.-284C>A
ENST00000413209.6:c.-284C>A ENSP00000409921.2:n.-284C>A
NM_000268.3:c.-284C>A , LRG_511t1:c.-284C>A NP_000259.1:n.-284C>A
NM_016418.5:c.-284C>A , LRG_511t2:c.-284C>A NP_057502.2:n.-284C>A
NM_181825.2:c.-284C>A NP_861546.1:n.-284C>A
NM_181828.2:c.-284C>A NP_861966.1:n.-284C>A
NM_181829.2:c.-284C>A NP_861967.1:n.-284C>A
NM_181830.2:c.-284C>A NP_861968.1:n.-284C>A
NM_181831.2:c.-284C>A NP_861969.1:n.-284C>A
NM_181832.2:c.-284C>A NP_861970.1:n.-284C>A
NM_181833.2:c.-284C>A NP_861971.1:n.-284C>A
NR_156186.1:n.160C>A
NM_000268.4:c.-284C>A MANE Select NP_000259.1:n.-284C>A
NM_181825.3:c.-284C>A NP_861546.1:n.-284C>A
NM_181828.3:c.-284C>A NP_861966.1:n.-284C>A
NM_181829.3:c.-284C>A NP_861967.1:n.-284C>A
NM_181830.3:c.-284C>A NP_861968.1:n.-284C>A
NM_181831.3:c.-284C>A NP_861969.1:n.-284C>A
NM_181832.3:c.-284C>A NP_861970.1:n.-284C>A
NR_156186.2:n.83C>A
NM_181833.3:c.-284C>A NP_861971.1:n.-284C>A