Canonical Allele Identifier: CA398994848
Gene: NF1 HGNC NCBI

Linked Data

dbSNP Id: rs2151451331

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31249003C>G , CM000679.2:g.31249003C>G GRCh38
NC_000017.10:g.29576021C>G , CM000679.1:g.29576021C>G GRCh37
NC_000017.9:g.26600147C>G NCBI36
NG_009018.1:g.159027C>G , LRG_214:g.159027C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.4039C>G ENSP00000512431.1:p.Leu1347Val
ENST00000696139.1:c.1457C>G ENSP00000512432.1:n.1457C>G
ENST00000696140.1:n.100C>G
ENST00000687863.1:n.702C>G
ENST00000691014.1:c.4024C>G ENSP00000510595.1:p.Leu1342Val
ENST00000358273.9:c.3994C>G MANE Select ENSP00000351015.4:p.Leu1332Val
ENST00000356175.7:c.3994C>G ENSP00000348498.3:p.Leu1332Val
ENST00000358273.8:c.3994C>G ENSP00000351015.4:p.Leu1332Val
ENST00000456735.6:c.2992C>G ENSP00000389907.2:p.Leu998Val
ENST00000466819.5:c.470C>G
ENST00000479614.1:c.470C>G
ENST00000493220.5:n.2530C>G
ENST00000495910.6:c.3769C>G
ENST00000579081.5:c.4096C>G ENSP00000462408.1:p.Leu1366Val
NM_000267.3:c.3994C>G , LRG_214t1:c.3994C>G NP_000258.1:p.Leu1332Val
NM_001042492.2:c.3994C>G , LRG_214t2:c.3994C>G NP_001035957.1:p.Leu1332Val
XM_005257983.1:c.3994C>G XP_005258040.1:p.Leu1332Val
XM_005257984.1:c.3994C>G XP_005258041.1:p.Leu1332Val
XM_006721922.1:c.4024C>G XP_006721985.1:p.Leu1342Val
XM_006721923.2:c.3985C>G XP_006721986.1:p.Leu1329Val
XM_006721924.1:c.4024C>G XP_006721987.1:p.Leu1342Val
XM_006721925.1:c.4024C>G XP_006721988.1:p.Leu1342Val
XM_006721926.2:c.4024C>G XP_006721989.1:p.Leu1342Val
XM_006721927.1:c.4024C>G XP_006721990.1:p.Leu1342Val
XM_006721928.2:c.4024C>G XP_006721991.1:p.Leu1342Val
XM_011524852.1:c.4021C>G XP_011523154.1:p.Leu1341Val
XM_011524853.1:c.3985C>G XP_011523155.1:p.Leu1329Val
XM_011524854.1:c.3985C>G XP_011523156.1:p.Leu1329Val
XM_011524855.1:c.3985C>G XP_011523157.1:p.Leu1329Val
XM_011524856.1:c.3985C>G XP_011523158.1:p.Leu1329Val
XM_011524857.1:c.4024C>G XP_011523159.1:p.Leu1342Val
NM_001042492.3:c.3994C>G MANE Select NP_001035957.1:p.Leu1332Val