Canonical Allele Identifier: CA399010523
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1044469
ClinVar RCV Id: RCV001348715
dbSNP Id: rs2069454728

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31330493A>G , CM000679.2:g.31330493A>G GRCh38
NC_000017.10:g.29657511A>G , CM000679.1:g.29657511A>G GRCh37
NC_000017.9:g.26681637A>G NCBI36
NG_009018.1:g.240517A>G , LRG_214:g.240517A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000581113.7:c.1995A>G ENSP00000492721.2:n.1995A>G
ENST00000696138.1:c.5789A>G ENSP00000512431.1:p.Lys1930Arg
ENST00000684826.1:c.371A>G ENSP00000509994.1:p.Lys124Arg
ENST00000687027.1:c.-38A>G ENSP00000508715.1:n.-38A>G
ENST00000687863.1:n.2452A>G
ENST00000691014.1:c.5837A>G ENSP00000510595.1:p.Lys1946Arg
ENST00000693617.1:c.371A>G ENSP00000510031.1:p.Lys124Arg
ENST00000358273.9:c.5807A>G MANE Select ENSP00000351015.4:p.Lys1936Arg
ENST00000356175.7:c.5744A>G ENSP00000348498.3:p.Lys1915Arg
ENST00000358273.8:c.5807A>G ENSP00000351015.4:p.Lys1936Arg
ENST00000456735.6:c.4742A>G ENSP00000389907.2:p.Lys1581Arg
ENST00000479536.2:c.165A>G
ENST00000493220.5:n.4280A>G
ENST00000579081.5:c.5943A>G ENSP00000462408.1:n.5943A>G
ENST00000581113.6:n.1124A>G
NM_000267.3:c.5744A>G , LRG_214t1:c.5744A>G NP_000258.1:p.Lys1915Arg
NM_001042492.2:c.5807A>G , LRG_214t2:c.5807A>G NP_001035957.1:p.Lys1936Arg
XM_005257983.1:c.5807A>G XP_005258040.1:p.Lys1936Arg
XM_005257984.1:c.5744A>G XP_005258041.1:p.Lys1915Arg
XM_006721922.1:c.5837A>G XP_006721985.1:p.Lys1946Arg
XM_006721923.2:c.5798A>G XP_006721986.1:p.Lys1933Arg
XM_006721924.1:c.5837A>G XP_006721987.1:p.Lys1946Arg
XM_006721925.1:c.5774A>G XP_006721988.1:p.Lys1925Arg
XM_006721926.2:c.5837A>G XP_006721989.1:p.Lys1946Arg
XM_006721927.1:c.5837A>G XP_006721990.1:p.Lys1946Arg
XM_011524852.1:c.5834A>G XP_011523154.1:p.Lys1945Arg
XM_011524853.1:c.5798A>G XP_011523155.1:p.Lys1933Arg
XM_011524854.1:c.5798A>G XP_011523156.1:p.Lys1933Arg
XM_011524855.1:c.5798A>G XP_011523157.1:p.Lys1933Arg
XM_011524856.1:c.5798A>G XP_011523158.1:p.Lys1933Arg
XM_011524857.1:c.5837A>G XP_011523159.1:p.Lys1946Arg
NM_001042492.3:c.5807A>G MANE Select NP_001035957.1:p.Lys1936Arg