Canonical Allele Identifier: CA2255577439

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31261804A= , CM000679.2:g.31261804A=	GRCh38
NC_000017.10:g.29588822A= , CM000679.1:g.29588822A=	GRCh37
NC_000017.9:g.26612948A=	NCBI36
NG_009018.1:g.171828A= , LRG_214:g.171828A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581113.7:c.473A=	ENSP00000492721.2:p.His158=
ENST00000696138.1:c.4653A=	ENSP00000512431.1:p.Thr1551=
ENST00000696140.1:n.777A=
ENST00000696141.1:c.662A=
ENST00000687863.1:n.1316A=
ENST00000691014.1:c.4701A=	ENSP00000510595.1:p.Thr1567=
ENST00000358273.9:c.4671A= MANE Select	ENSP00000351015.4:p.Thr1557=
ENST00000356175.7:c.4608A=	ENSP00000348498.3:p.Thr1536=
ENST00000358273.8:c.4671A=	ENSP00000351015.4:p.Thr1557=
ENST00000456735.6:c.3606A=	ENSP00000389907.2:p.Thr1202=
ENST00000493220.5:n.3144A=
ENST00000579081.5:c.4710A=	ENSP00000462408.1:p.Thr1570=
NM_000267.3:c.4608A= , LRG_214t1:c.4608A=	NP_000258.1:p.Thr1536=
NM_001042492.2:c.4671A= , LRG_214t2:c.4671A=	NP_001035957.1:p.Thr1557=
XM_005257983.1:c.4671A=	XP_005258040.1:p.Thr1557=
XM_005257984.1:c.4608A=	XP_005258041.1:p.Thr1536=
XM_006721922.1:c.4701A=	XP_006721985.1:p.Thr1567=
XM_006721923.2:c.4662A=	XP_006721986.1:p.Thr1554=
XM_006721924.1:c.4701A=	XP_006721987.1:p.Thr1567=
XM_006721925.1:c.4638A=	XP_006721988.1:p.Thr1546=
XM_006721926.2:c.4701A=	XP_006721989.1:p.Thr1567=
XM_006721927.1:c.4701A=	XP_006721990.1:p.Thr1567=
XM_006721928.2:c.4701A=	XP_006721991.1:p.Thr1567=
XM_011524852.1:c.4698A=	XP_011523154.1:p.Thr1566=
XM_011524853.1:c.4662A=	XP_011523155.1:p.Thr1554=
XM_011524854.1:c.4662A=	XP_011523156.1:p.Thr1554=
XM_011524855.1:c.4662A=	XP_011523157.1:p.Thr1554=
XM_011524856.1:c.4662A=	XP_011523158.1:p.Thr1554=
XM_011524857.1:c.4701A=	XP_011523159.1:p.Thr1567=
NM_001042492.3:c.4671A= MANE Select	NP_001035957.1:p.Thr1557=