Canonical Allele Identifier: CA2255605132

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31343126C= , CM000679.2:g.31343126C=	GRCh38
NC_000017.10:g.29670144C= , CM000679.1:g.29670144C=	GRCh37
NC_000017.9:g.26694270C=	NCBI36
NG_009018.1:g.253150C= , LRG_214:g.253150C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7162C=	ENSP00000512431.1:p.Leu2388=
ENST00000684826.1:c.1744C=	ENSP00000509994.1:p.Leu582=
ENST00000687027.1:c.1336C=	ENSP00000508715.1:p.Leu446=
ENST00000687863.1:n.3825C=
ENST00000689464.1:c.119C=
ENST00000691014.1:c.7210C=	ENSP00000510595.1:p.Leu2404=
ENST00000693617.1:c.1744C=	ENSP00000510031.1:p.Leu582=
ENST00000358273.9:c.7180C= MANE Select	ENSP00000351015.4:p.Leu2394=
ENST00000356175.7:c.7117C=	ENSP00000348498.3:p.Leu2373=
ENST00000358273.8:c.7180C=	ENSP00000351015.4:p.Leu2394=
ENST00000456735.6:c.6115C=	ENSP00000389907.2:p.Leu2039=
ENST00000471572.6:c.563C=
ENST00000579081.5:c.7316C=	ENSP00000462408.1:n.7316C=
ENST00000581790.5:c.323C=
ENST00000582892.1:n.422C=
NM_000267.3:c.7117C= , LRG_214t1:c.7117C=	NP_000258.1:p.Leu2373=
NM_001042492.2:c.7180C= , LRG_214t2:c.7180C=	NP_001035957.1:p.Leu2394=
XM_005257983.1:c.7180C=	XP_005258040.1:p.Leu2394=
XM_005257984.1:c.7117C=	XP_005258041.1:p.Leu2373=
XM_006721922.1:c.7210C=	XP_006721985.1:p.Leu2404=
XM_006721923.2:c.7171C=	XP_006721986.1:p.Leu2391=
XM_006721924.1:c.7210C=	XP_006721987.1:p.Leu2404=
XM_006721925.1:c.7147C=	XP_006721988.1:p.Leu2383=
XM_006721926.2:c.7210C=	XP_006721989.1:p.Leu2404=
XM_006721927.1:c.7210C=	XP_006721990.1:p.Leu2404=
XM_011524852.1:c.7207C=	XP_011523154.1:p.Leu2403=
XM_011524853.1:c.7171C=	XP_011523155.1:p.Leu2391=
XM_011524854.1:c.7171C=	XP_011523156.1:p.Leu2391=
XM_011524855.1:c.7171C=	XP_011523157.1:p.Leu2391=
XM_011524856.1:c.7171C=	XP_011523158.1:p.Leu2391=
XM_011524857.1:c.7210C=	XP_011523159.1:p.Leu2404=
NM_001042492.3:c.7180C= MANE Select	NP_001035957.1:p.Leu2394=