Canonical Allele Identifier: CA2255566557
Gene: NF1 HGNC NCBI

Linked Data

dbSNP Id: rs2067447860

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31248995dup , CM000679.2:g.31248995dup GRCh38
NC_000017.10:g.29576013dup , CM000679.1:g.29576013dup GRCh37
NC_000017.9:g.26600139dup NCBI36
NG_009018.1:g.159019dup , LRG_214:g.159019dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.4031dup ENSP00000512431.1:p.Glu1345ArgfsTer4
ENST00000696139.1:c.1449dup ENSP00000512432.1:n.1449dup
ENST00000696140.1:n.92dup
ENST00000687863.1:n.694dup
ENST00000691014.1:c.4016dup ENSP00000510595.1:p.Glu1340ArgfsTer4
ENST00000358273.9:c.3986dup MANE Select ENSP00000351015.4:p.Glu1330ArgfsTer4
ENST00000356175.7:c.3986dup ENSP00000348498.3:p.Glu1330ArgfsTer4
ENST00000358273.8:c.3986dup ENSP00000351015.4:p.Glu1330ArgfsTer4
ENST00000456735.6:c.2984dup ENSP00000389907.2:p.Glu996ArgfsTer4
ENST00000466819.5:c.462dup
ENST00000479614.1:c.462dup
ENST00000493220.5:n.2522dup
ENST00000495910.6:c.3761dup
ENST00000579081.5:c.4088dup ENSP00000462408.1:p.Glu1364ArgfsTer4
NM_000267.3:c.3986dup , LRG_214t1:c.3986dup NP_000258.1:p.Glu1330ArgfsTer4
NM_001042492.2:c.3986dup , LRG_214t2:c.3986dup NP_001035957.1:p.Glu1330ArgfsTer4
XM_005257983.1:c.3986dup XP_005258040.1:p.Glu1330ArgfsTer4
XM_005257984.1:c.3986dup XP_005258041.1:p.Glu1330ArgfsTer4
XM_006721922.1:c.4016dup XP_006721985.1:p.Glu1340ArgfsTer4
XM_006721923.2:c.3977dup XP_006721986.1:p.Glu1327ArgfsTer4
XM_006721924.1:c.4016dup XP_006721987.1:p.Glu1340ArgfsTer4
XM_006721925.1:c.4016dup XP_006721988.1:p.Glu1340ArgfsTer4
XM_006721926.2:c.4016dup XP_006721989.1:p.Glu1340ArgfsTer4
XM_006721927.1:c.4016dup XP_006721990.1:p.Glu1340ArgfsTer4
XM_006721928.2:c.4016dup XP_006721991.1:p.Glu1340ArgfsTer4
XM_011524852.1:c.4013dup XP_011523154.1:p.Glu1339ArgfsTer4
XM_011524853.1:c.3977dup XP_011523155.1:p.Glu1327ArgfsTer4
XM_011524854.1:c.3977dup XP_011523156.1:p.Glu1327ArgfsTer4
XM_011524855.1:c.3977dup XP_011523157.1:p.Glu1327ArgfsTer4
XM_011524856.1:c.3977dup XP_011523158.1:p.Glu1327ArgfsTer4
XM_011524857.1:c.4016dup XP_011523159.1:p.Glu1340ArgfsTer4
NM_001042492.3:c.3986dup MANE Select NP_001035957.1:p.Glu1330ArgfsTer4