Canonical Allele Identifier: CA2255603114

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31338712G= , CM000679.2:g.31338712G=	GRCh38
NC_000017.10:g.29665730G= , CM000679.1:g.29665730G=	GRCh37
NC_000017.9:g.26689856G=	NCBI36
NG_009018.1:g.248736G= , LRG_214:g.248736G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.6810G=	ENSP00000512431.1:p.Glu2270=
ENST00000684826.1:c.1392G=	ENSP00000509994.1:p.Glu464=
ENST00000684998.1:n.2650G=
ENST00000687027.1:c.984G=	ENSP00000508715.1:p.Glu328=
ENST00000687863.1:n.3473G=
ENST00000691014.1:c.6858G=	ENSP00000510595.1:p.Glu2286=
ENST00000693617.1:c.1392G=	ENSP00000510031.1:p.Glu464=
ENST00000358273.9:c.6828G= MANE Select	ENSP00000351015.4:p.Glu2276=
ENST00000356175.7:c.6765G=	ENSP00000348498.3:p.Glu2255=
ENST00000358273.8:c.6828G=	ENSP00000351015.4:p.Glu2276=
ENST00000456735.6:c.5763G=	ENSP00000389907.2:p.Glu1921=
ENST00000471572.6:c.211G=
ENST00000579081.5:c.6964G=	ENSP00000462408.1:n.6964G=
ENST00000581790.5:c.64+832G=
ENST00000584328.1:n.242G=
NM_000267.3:c.6765G= , LRG_214t1:c.6765G=	NP_000258.1:p.Glu2255=
NM_001042492.2:c.6828G= , LRG_214t2:c.6828G=	NP_001035957.1:p.Glu2276=
XM_005257983.1:c.6828G=	XP_005258040.1:p.Glu2276=
XM_005257984.1:c.6765G=	XP_005258041.1:p.Glu2255=
XM_006721922.1:c.6858G=	XP_006721985.1:p.Glu2286=
XM_006721923.2:c.6819G=	XP_006721986.1:p.Glu2273=
XM_006721924.1:c.6858G=	XP_006721987.1:p.Glu2286=
XM_006721925.1:c.6795G=	XP_006721988.1:p.Glu2265=
XM_006721926.2:c.6858G=	XP_006721989.1:p.Glu2286=
XM_006721927.1:c.6858G=	XP_006721990.1:p.Glu2286=
XM_011524852.1:c.6855G=	XP_011523154.1:p.Glu2285=
XM_011524853.1:c.6819G=	XP_011523155.1:p.Glu2273=
XM_011524854.1:c.6819G=	XP_011523156.1:p.Glu2273=
XM_011524855.1:c.6819G=	XP_011523157.1:p.Glu2273=
XM_011524856.1:c.6819G=	XP_011523158.1:p.Glu2273=
XM_011524857.1:c.6858G=	XP_011523159.1:p.Glu2286=
NM_001042492.3:c.6828G= MANE Select	NP_001035957.1:p.Glu2276=