Canonical Allele Identifier: CA2255603147

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31338765C= , CM000679.2:g.31338765C=	GRCh38
NC_000017.10:g.29665783C= , CM000679.1:g.29665783C=	GRCh37
NC_000017.9:g.26689909C=	NCBI36
NG_009018.1:g.248789C= , LRG_214:g.248789C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.6863C=	ENSP00000512431.1:p.Thr2288=
ENST00000684826.1:c.1445C=	ENSP00000509994.1:p.Thr482=
ENST00000684998.1:n.2703C=
ENST00000687027.1:c.1037C=	ENSP00000508715.1:p.Thr346=
ENST00000687863.1:n.3526C=
ENST00000691014.1:c.6911C=	ENSP00000510595.1:p.Thr2304=
ENST00000693617.1:c.1445C=	ENSP00000510031.1:p.Thr482=
ENST00000358273.9:c.6881C= MANE Select	ENSP00000351015.4:p.Thr2294=
ENST00000356175.7:c.6818C=	ENSP00000348498.3:p.Thr2273=
ENST00000358273.8:c.6881C=	ENSP00000351015.4:p.Thr2294=
ENST00000456735.6:c.5816C=	ENSP00000389907.2:p.Thr1939=
ENST00000471572.6:c.264C=
ENST00000579081.5:c.7017C=	ENSP00000462408.1:n.7017C=
ENST00000581790.5:c.64+885C=
ENST00000584328.1:n.295C=
NM_000267.3:c.6818C= , LRG_214t1:c.6818C=	NP_000258.1:p.Thr2273=
NM_001042492.2:c.6881C= , LRG_214t2:c.6881C=	NP_001035957.1:p.Thr2294=
XM_005257983.1:c.6881C=	XP_005258040.1:p.Thr2294=
XM_005257984.1:c.6818C=	XP_005258041.1:p.Thr2273=
XM_006721922.1:c.6911C=	XP_006721985.1:p.Thr2304=
XM_006721923.2:c.6872C=	XP_006721986.1:p.Thr2291=
XM_006721924.1:c.6911C=	XP_006721987.1:p.Thr2304=
XM_006721925.1:c.6848C=	XP_006721988.1:p.Thr2283=
XM_006721926.2:c.6911C=	XP_006721989.1:p.Thr2304=
XM_006721927.1:c.6911C=	XP_006721990.1:p.Thr2304=
XM_011524852.1:c.6908C=	XP_011523154.1:p.Thr2303=
XM_011524853.1:c.6872C=	XP_011523155.1:p.Thr2291=
XM_011524854.1:c.6872C=	XP_011523156.1:p.Thr2291=
XM_011524855.1:c.6872C=	XP_011523157.1:p.Thr2291=
XM_011524856.1:c.6872C=	XP_011523158.1:p.Thr2291=
XM_011524857.1:c.6911C=	XP_011523159.1:p.Thr2304=
NM_001042492.3:c.6881C= MANE Select	NP_001035957.1:p.Thr2294=