Canonical Allele Identifier: CA2255572905

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31235665C= , CM000679.2:g.31235665C=	GRCh38
NC_000017.10:g.29562683C= , CM000679.1:g.29562683C=	GRCh37
NC_000017.9:g.26586809C=	NCBI36
NG_009018.1:g.145689C= , LRG_214:g.145689C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001042492.3:c.3763C= MANE Select	NP_001035957.1:p.Gln1255=
ENST00000358273.9:c.3763C= MANE Select	ENSP00000351015.4:p.Gln1255=
NM_000267.3:c.3763C= , LRG_214t1:c.3763C=	NP_000258.1:p.Gln1255=
NM_001042492.2:c.3763C= , LRG_214t2:c.3763C=	NP_001035957.1:p.Gln1255=
ENST00000356175.7:c.3763C=	ENSP00000348498.3:p.Gln1255=
ENST00000358273.8:c.3763C=	ENSP00000351015.4:p.Gln1255=
ENST00000456735.6:c.2761C=	ENSP00000389907.2:p.Gln921=
ENST00000466819.5:c.239C=
ENST00000479614.1:c.239C=
ENST00000493220.5:n.2299C=
ENST00000495910.6:c.3538C=
ENST00000579081.5:c.3865C=	ENSP00000462408.1:p.Gln1289=
ENST00000687863.1:n.471C=
ENST00000691014.1:c.3793C=	ENSP00000510595.1:p.Gln1265=
ENST00000696138.1:c.3808C=	ENSP00000512431.1:p.Gln1270=
ENST00000696139.1:c.1108C=	ENSP00000512432.1:p.Gln370=
XM_005257983.1:c.3763C=	XP_005258040.1:p.Gln1255=
XM_005257984.1:c.3763C=	XP_005258041.1:p.Gln1255=
XM_006721922.1:c.3793C=	XP_006721985.1:p.Gln1265=
XM_006721923.2:c.3754C=	XP_006721986.1:p.Gln1252=
XM_006721924.1:c.3793C=	XP_006721987.1:p.Gln1265=
XM_006721925.1:c.3793C=	XP_006721988.1:p.Gln1265=
XM_006721926.2:c.3793C=	XP_006721989.1:p.Gln1265=
XM_006721927.1:c.3793C=	XP_006721990.1:p.Gln1265=
XM_006721928.2:c.3793C=	XP_006721991.1:p.Gln1265=
XM_011524852.1:c.3790C=	XP_011523154.1:p.Gln1264=
XM_011524853.1:c.3754C=	XP_011523155.1:p.Gln1252=
XM_011524854.1:c.3754C=	XP_011523156.1:p.Gln1252=
XM_011524855.1:c.3754C=	XP_011523157.1:p.Gln1252=
XM_011524856.1:c.3754C=	XP_011523158.1:p.Gln1252=
XM_011524857.1:c.3793C=	XP_011523159.1:p.Gln1265=