Canonical Allele Identifier: CA2255614254

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31357025A= , CM000679.2:g.31357025A=	GRCh38
NC_000017.10:g.29684043A= , CM000679.1:g.29684043A=	GRCh37
NC_000017.9:g.26708169A=	NCBI36
NG_009018.1:g.267049A= , LRG_214:g.267049A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7786A=	ENSP00000512431.1:p.Asn2596=
ENST00000684826.1:c.2368A=	ENSP00000509994.1:p.Asn790=
ENST00000687027.1:c.1960A=	ENSP00000508715.1:p.Asn654=
ENST00000687863.1:n.4449A=
ENST00000689464.1:c.854A=
ENST00000691014.1:c.7834A=	ENSP00000510595.1:p.Asn2612=
ENST00000693617.1:c.2368A=	ENSP00000510031.1:p.Asn790=
ENST00000358273.9:c.7804A= MANE Select	ENSP00000351015.4:p.Asn2602=
ENST00000356175.7:c.7741A=	ENSP00000348498.3:p.Asn2581=
ENST00000358273.8:c.7804A=	ENSP00000351015.4:p.Asn2602=
ENST00000456735.6:c.6739A=	ENSP00000389907.2:p.Asn2247=
ENST00000471572.6:c.1187A=
ENST00000577967.1:n.1222A=
ENST00000579081.5:c.7940A=	ENSP00000462408.1:n.7940A=
ENST00000581790.5:c.789A=
NM_000267.3:c.7741A= , LRG_214t1:c.7741A=	NP_000258.1:p.Asn2581=
NM_001042492.2:c.7804A= , LRG_214t2:c.7804A=	NP_001035957.1:p.Asn2602=
XM_005257983.1:c.7804A=	XP_005258040.1:p.Asn2602=
XM_005257984.1:c.7741A=	XP_005258041.1:p.Asn2581=
XM_006721922.1:c.7834A=	XP_006721985.1:p.Asn2612=
XM_006721923.2:c.7795A=	XP_006721986.1:p.Asn2599=
XM_006721924.1:c.7834A=	XP_006721987.1:p.Asn2612=
XM_006721925.1:c.7771A=	XP_006721988.1:p.Asn2591=
XM_006721926.2:c.7834A=	XP_006721989.1:p.Asn2612=
XM_006721927.1:c.7834A=	XP_006721990.1:p.Asn2612=
XM_011524852.1:c.7831A=	XP_011523154.1:p.Asn2611=
XM_011524853.1:c.7795A=	XP_011523155.1:p.Asn2599=
XM_011524854.1:c.7795A=	XP_011523156.1:p.Asn2599=
XM_011524855.1:c.7795A=	XP_011523157.1:p.Asn2599=
XM_011524856.1:c.7795A=	XP_011523158.1:p.Asn2599=
XM_011524857.1:c.7711A=	XP_011523159.1:p.Asn2571=
NM_001042492.3:c.7804A= MANE Select	NP_001035957.1:p.Asn2602=