Canonical Allele Identifier: CA2255570746

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31233170C= , CM000679.2:g.31233170C=	GRCh38
NC_000017.10:g.29560188C= , CM000679.1:g.29560188C=	GRCh37
NC_000017.9:g.26584314C=	NCBI36
NG_009018.1:g.143194C= , LRG_214:g.143194C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.3710C=	ENSP00000512431.1:p.Pro1237=
ENST00000696139.1:c.1010C=	ENSP00000512432.1:p.Pro337=
ENST00000691014.1:c.3695C=	ENSP00000510595.1:p.Pro1232=
ENST00000693210.1:n.391C=
ENST00000358273.9:c.3665C= MANE Select	ENSP00000351015.4:p.Pro1222=
ENST00000356175.7:c.3665C=	ENSP00000348498.3:p.Pro1222=
ENST00000358273.8:c.3665C=	ENSP00000351015.4:p.Pro1222=
ENST00000456735.6:c.2663C=	ENSP00000389907.2:p.Pro888=
ENST00000466819.5:c.141C=
ENST00000479614.1:c.141C=
ENST00000493220.5:n.2201C=
ENST00000495910.6:c.3440C=
ENST00000579081.5:c.3767C=	ENSP00000462408.1:p.Pro1256=
NM_000267.3:c.3665C= , LRG_214t1:c.3665C=	NP_000258.1:p.Pro1222=
NM_001042492.2:c.3665C= , LRG_214t2:c.3665C=	NP_001035957.1:p.Pro1222=
XM_005257983.1:c.3665C=	XP_005258040.1:p.Pro1222=
XM_005257984.1:c.3665C=	XP_005258041.1:p.Pro1222=
XM_006721922.1:c.3695C=	XP_006721985.1:p.Pro1232=
XM_006721923.2:c.3656C=	XP_006721986.1:p.Pro1219=
XM_006721924.1:c.3695C=	XP_006721987.1:p.Pro1232=
XM_006721925.1:c.3695C=	XP_006721988.1:p.Pro1232=
XM_006721926.2:c.3695C=	XP_006721989.1:p.Pro1232=
XM_006721927.1:c.3695C=	XP_006721990.1:p.Pro1232=
XM_006721928.2:c.3695C=	XP_006721991.1:p.Pro1232=
XM_011524852.1:c.3692C=	XP_011523154.1:p.Pro1231=
XM_011524853.1:c.3656C=	XP_011523155.1:p.Pro1219=
XM_011524854.1:c.3656C=	XP_011523156.1:p.Pro1219=
XM_011524855.1:c.3656C=	XP_011523157.1:p.Pro1219=
XM_011524856.1:c.3656C=	XP_011523158.1:p.Pro1219=
XM_011524857.1:c.3695C=	XP_011523159.1:p.Pro1232=
NM_001042492.3:c.3665C= MANE Select	NP_001035957.1:p.Pro1222=