Canonical Allele Identifier: CA2255578958
Gene: NF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31265266A= , CM000679.2:g.31265266A= GRCh38
NC_000017.10:g.29592284A= , CM000679.1:g.29592284A= GRCh37
NC_000017.9:g.26616410A= NCBI36
NG_009018.1:g.175290A= , LRG_214:g.175290A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000581113.7:c.564A= ENSP00000492721.2:n.564A=
ENST00000696138.1:c.4744A= ENSP00000512431.1:p.Lys1582=
ENST00000696140.1:n.868A=
ENST00000696141.1:c.753A=
ENST00000687863.1:n.1407A=
ENST00000691014.1:c.4792A= ENSP00000510595.1:p.Lys1598=
ENST00000358273.9:c.4762A= MANE Select ENSP00000351015.4:p.Lys1588=
ENST00000356175.7:c.4699A= ENSP00000348498.3:p.Lys1567=
ENST00000358273.8:c.4762A= ENSP00000351015.4:p.Lys1588=
ENST00000456735.6:c.3697A= ENSP00000389907.2:p.Lys1233=
ENST00000493220.5:n.3235A=
ENST00000579081.5:c.4801A= ENSP00000462408.1:p.Lys1601=
NM_000267.3:c.4699A= , LRG_214t1:c.4699A= NP_000258.1:p.Lys1567=
NM_001042492.2:c.4762A= , LRG_214t2:c.4762A= NP_001035957.1:p.Lys1588=
XM_005257983.1:c.4762A= XP_005258040.1:p.Lys1588=
XM_005257984.1:c.4699A= XP_005258041.1:p.Lys1567=
XM_006721922.1:c.4792A= XP_006721985.1:p.Lys1598=
XM_006721923.2:c.4753A= XP_006721986.1:p.Lys1585=
XM_006721924.1:c.4792A= XP_006721987.1:p.Lys1598=
XM_006721925.1:c.4729A= XP_006721988.1:p.Lys1577=
XM_006721926.2:c.4792A= XP_006721989.1:p.Lys1598=
XM_006721927.1:c.4792A= XP_006721990.1:p.Lys1598=
XM_006721928.2:c.4792A= XP_006721991.1:p.Lys1598=
XM_011524852.1:c.4789A= XP_011523154.1:p.Lys1597=
XM_011524853.1:c.4753A= XP_011523155.1:p.Lys1585=
XM_011524854.1:c.4753A= XP_011523156.1:p.Lys1585=
XM_011524855.1:c.4753A= XP_011523157.1:p.Lys1585=
XM_011524856.1:c.4753A= XP_011523158.1:p.Lys1585=
XM_011524857.1:c.4792A= XP_011523159.1:p.Lys1598=
NM_001042492.3:c.4762A= MANE Select NP_001035957.1:p.Lys1588=