Canonical Allele Identifier: CA398995050
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2762236
ClinVar RCV Id: RCV003496019
dbSNP Id: rs137854560

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31249093C>G , CM000679.2:g.31249093C>G GRCh38
NC_000017.10:g.29576111C>G , CM000679.1:g.29576111C>G GRCh37
NC_000017.9:g.26600237C>G NCBI36
NG_009018.1:g.159117C>G , LRG_214:g.159117C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696138.1:c.4129C>G ENSP00000512431.1:p.Arg1377Gly
ENST00000696139.1:c.1547C>G ENSP00000512432.1:n.1547C>G
ENST00000696140.1:n.190C>G
ENST00000687863.1:n.792C>G
ENST00000691014.1:c.4114C>G ENSP00000510595.1:p.Arg1372Gly
ENST00000358273.9:c.4084C>G MANE Select ENSP00000351015.4:p.Arg1362Gly
ENST00000356175.7:c.4084C>G ENSP00000348498.3:p.Arg1362Gly
ENST00000358273.8:c.4084C>G ENSP00000351015.4:p.Arg1362Gly
ENST00000456735.6:c.3082C>G ENSP00000389907.2:p.Arg1028Gly
ENST00000466819.5:c.560C>G
ENST00000479614.1:c.560C>G
ENST00000493220.5:n.2620C>G
ENST00000495910.6:c.3859C>G
ENST00000579081.5:c.4186C>G ENSP00000462408.1:p.Arg1396Gly
NM_000267.3:c.4084C>G , LRG_214t1:c.4084C>G NP_000258.1:p.Arg1362Gly
NM_001042492.2:c.4084C>G , LRG_214t2:c.4084C>G NP_001035957.1:p.Arg1362Gly
XM_005257983.1:c.4084C>G XP_005258040.1:p.Arg1362Gly
XM_005257984.1:c.4084C>G XP_005258041.1:p.Arg1362Gly
XM_006721922.1:c.4114C>G XP_006721985.1:p.Arg1372Gly
XM_006721923.2:c.4075C>G XP_006721986.1:p.Arg1359Gly
XM_006721924.1:c.4114C>G XP_006721987.1:p.Arg1372Gly
XM_006721925.1:c.4114C>G XP_006721988.1:p.Arg1372Gly
XM_006721926.2:c.4114C>G XP_006721989.1:p.Arg1372Gly
XM_006721927.1:c.4114C>G XP_006721990.1:p.Arg1372Gly
XM_006721928.2:c.4114C>G XP_006721991.1:p.Arg1372Gly
XM_011524852.1:c.4111C>G XP_011523154.1:p.Arg1371Gly
XM_011524853.1:c.4075C>G XP_011523155.1:p.Arg1359Gly
XM_011524854.1:c.4075C>G XP_011523156.1:p.Arg1359Gly
XM_011524855.1:c.4075C>G XP_011523157.1:p.Arg1359Gly
XM_011524856.1:c.4075C>G XP_011523158.1:p.Arg1359Gly
XM_011524857.1:c.4114C>G XP_011523159.1:p.Arg1372Gly
NM_001042492.3:c.4084C>G MANE Select NP_001035957.1:p.Arg1362Gly