Canonical Allele Identifier: CA2573153638
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1394572
dbSNP Id: rs2143959373

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31214508del , CM000679.2:g.31214508del GRCh38
NC_000017.10:g.29541526del , CM000679.1:g.29541526del GRCh37
NC_000017.9:g.26565652del NCBI36
NG_009018.1:g.124532del , LRG_214:g.124532del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.1495del ENSP00000512431.1:p.Leu499TrpfsTer14
ENST00000686189.1:c.895del ENSP00000509682.1:p.Leu299TrpfsTer14
ENST00000691014.1:c.1480del ENSP00000510595.1:p.Leu494TrpfsTer14
ENST00000358273.9:c.1450del MANE Select ENSP00000351015.4:p.Leu484TrpfsTer14
ENST00000356175.7:c.1450del ENSP00000348498.3:p.Leu484TrpfsTer14
ENST00000358273.8:c.1450del ENSP00000351015.4:p.Leu484TrpfsTer14
ENST00000431387.8:c.1450del ENSP00000412921.4:p.Leu484TrpfsTer14
ENST00000456735.6:c.448del ENSP00000389907.2:p.Leu150TrpfsTer14
ENST00000487476.5:n.1833del
ENST00000495910.6:c.1225del
ENST00000579081.5:c.1552del ENSP00000462408.1:p.Leu518TrpfsTer14
NM_000267.3:c.1450del , LRG_214t1:c.1450del NP_000258.1:p.Leu484TrpfsTer14
NM_001042492.2:c.1450del , LRG_214t2:c.1450del NP_001035957.1:p.Leu484TrpfsTer14
NM_001128147.2:c.1450del NP_001121619.1:p.Leu484TrpfsTer14
XM_005257983.1:c.1450del XP_005258040.1:p.Leu484TrpfsTer14
XM_005257984.1:c.1450del XP_005258041.1:p.Leu484TrpfsTer14
XM_006721922.1:c.1480del XP_006721985.1:p.Leu494TrpfsTer14
XM_006721923.2:c.1441del XP_006721986.1:p.Leu481TrpfsTer14
XM_006721924.1:c.1480del XP_006721987.1:p.Leu494TrpfsTer14
XM_006721925.1:c.1480del XP_006721988.1:p.Leu494TrpfsTer14
XM_006721926.2:c.1480del XP_006721989.1:p.Leu494TrpfsTer14
XM_006721927.1:c.1480del XP_006721990.1:p.Leu494TrpfsTer14
XM_006721928.2:c.1480del XP_006721991.1:p.Leu494TrpfsTer14
XM_011524852.1:c.1480del XP_011523154.1:p.Leu494TrpfsTer14
XM_011524853.1:c.1441del XP_011523155.1:p.Leu481TrpfsTer14
XM_011524854.1:c.1441del XP_011523156.1:p.Leu481TrpfsTer14
XM_011524855.1:c.1441del XP_011523157.1:p.Leu481TrpfsTer14
XM_011524856.1:c.1441del XP_011523158.1:p.Leu481TrpfsTer14
XM_011524857.1:c.1480del XP_011523159.1:p.Leu494TrpfsTer14
NM_001042492.3:c.1450del MANE Select NP_001035957.1:p.Leu484TrpfsTer14
NM_001128147.3:c.1450del NP_001121619.1:p.Leu484TrpfsTer14