Canonical Allele Identifier: CA2255578946
Gene: NF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31265242G= , CM000679.2:g.31265242G= GRCh38
NC_000017.10:g.29592260G= , CM000679.1:g.29592260G= GRCh37
NC_000017.9:g.26616386G= NCBI36
NG_009018.1:g.175266G= , LRG_214:g.175266G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000581113.7:c.540G= ENSP00000492721.2:n.540G=
ENST00000696138.1:c.4720G= ENSP00000512431.1:p.Glu1574=
ENST00000696140.1:n.844G=
ENST00000696141.1:c.729G=
ENST00000687863.1:n.1383G=
ENST00000691014.1:c.4768G= ENSP00000510595.1:p.Glu1590=
ENST00000358273.9:c.4738G= MANE Select ENSP00000351015.4:p.Glu1580=
ENST00000356175.7:c.4675G= ENSP00000348498.3:p.Glu1559=
ENST00000358273.8:c.4738G= ENSP00000351015.4:p.Glu1580=
ENST00000456735.6:c.3673G= ENSP00000389907.2:p.Glu1225=
ENST00000493220.5:n.3211G=
ENST00000579081.5:c.4777G= ENSP00000462408.1:p.Glu1593=
NM_000267.3:c.4675G= , LRG_214t1:c.4675G= NP_000258.1:p.Glu1559=
NM_001042492.2:c.4738G= , LRG_214t2:c.4738G= NP_001035957.1:p.Glu1580=
XM_005257983.1:c.4738G= XP_005258040.1:p.Glu1580=
XM_005257984.1:c.4675G= XP_005258041.1:p.Glu1559=
XM_006721922.1:c.4768G= XP_006721985.1:p.Glu1590=
XM_006721923.2:c.4729G= XP_006721986.1:p.Glu1577=
XM_006721924.1:c.4768G= XP_006721987.1:p.Glu1590=
XM_006721925.1:c.4705G= XP_006721988.1:p.Glu1569=
XM_006721926.2:c.4768G= XP_006721989.1:p.Glu1590=
XM_006721927.1:c.4768G= XP_006721990.1:p.Glu1590=
XM_006721928.2:c.4768G= XP_006721991.1:p.Glu1590=
XM_011524852.1:c.4765G= XP_011523154.1:p.Glu1589=
XM_011524853.1:c.4729G= XP_011523155.1:p.Glu1577=
XM_011524854.1:c.4729G= XP_011523156.1:p.Glu1577=
XM_011524855.1:c.4729G= XP_011523157.1:p.Glu1577=
XM_011524856.1:c.4729G= XP_011523158.1:p.Glu1577=
XM_011524857.1:c.4768G= XP_011523159.1:p.Glu1590=
NM_001042492.3:c.4738G= MANE Select NP_001035957.1:p.Glu1580=