Canonical Allele Identifier: CA166117
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141682
ClinVar RCV Id: RCV000130296
dbSNP Id: rs587781933

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31229237_31229238insA , CM000679.2:g.31229237_31229238insA GRCh38
NC_000017.10:g.29556255_29556256insA , CM000679.1:g.29556255_29556256insA GRCh37
NC_000017.9:g.26580381_26580382insA NCBI36
NG_009018.1:g.139261_139262insA , LRG_214:g.139261_139262insA

Transcript Alleles

HGVS Amino-acid change
ENST00000696138.1:c.2667_2668insA ENSP00000512431.1:p.Gly890ArgfsTer?
ENST00000691014.1:c.2652_2653insA ENSP00000510595.1:p.Gly885ArgfsTer?
ENST00000358273.9:c.2622_2623insA MANE Select ENSP00000351015.4:p.Gly875ArgfsTer?
ENST00000356175.7:c.2622_2623insA ENSP00000348498.3:p.Gly875ArgfsTer?
ENST00000358273.8:c.2622_2623insA ENSP00000351015.4:p.Gly875ArgfsTer?
ENST00000456735.6:c.1620_1621insA ENSP00000389907.2:p.Gly541ArgfsTer?
ENST00000493220.5:n.789_790insA
ENST00000495910.6:c.2397_2398insA
ENST00000579081.5:c.2724_2725insA ENSP00000462408.1:p.Gly909ArgfsTer?
NM_000267.3:c.2622_2623insA , LRG_214t1:c.2622_2623insA NP_000258.1:p.Gly875ArgfsTer?
NM_001042492.2:c.2622_2623insA , LRG_214t2:c.2622_2623insA NP_001035957.1:p.Gly875ArgfsTer?
XM_005257983.1:c.2622_2623insA XP_005258040.1:p.Gly875ArgfsTer?
XM_005257984.1:c.2622_2623insA XP_005258041.1:p.Gly875ArgfsTer?
XM_006721922.1:c.2652_2653insA XP_006721985.1:p.Gly885ArgfsTer?
XM_006721923.2:c.2613_2614insA XP_006721986.1:p.Gly872ArgfsTer?
XM_006721924.1:c.2652_2653insA XP_006721987.1:p.Gly885ArgfsTer?
XM_006721925.1:c.2652_2653insA XP_006721988.1:p.Gly885ArgfsTer?
XM_006721926.2:c.2652_2653insA XP_006721989.1:p.Gly885ArgfsTer?
XM_006721927.1:c.2652_2653insA XP_006721990.1:p.Gly885ArgfsTer?
XM_006721928.2:c.2652_2653insA XP_006721991.1:p.Gly885ArgfsTer?
XM_011524852.1:c.2649_2650insA XP_011523154.1:p.Gly884ArgfsTer?
XM_011524853.1:c.2613_2614insA XP_011523155.1:p.Gly872ArgfsTer?
XM_011524854.1:c.2613_2614insA XP_011523156.1:p.Gly872ArgfsTer?
XM_011524855.1:c.2613_2614insA XP_011523157.1:p.Gly872ArgfsTer?
XM_011524856.1:c.2613_2614insA XP_011523158.1:p.Gly872ArgfsTer?
XM_011524857.1:c.2652_2653insA XP_011523159.1:p.Gly885ArgfsTer?
NM_001042492.3:c.2622_2623insA MANE Select NP_001035957.1:p.Gly875ArgfsTer?