Canonical Allele Identifier: CA2255605054

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31343013C= , CM000679.2:g.31343013C=	GRCh38
NC_000017.10:g.29670031C= , CM000679.1:g.29670031C=	GRCh37
NC_000017.9:g.26694157C=	NCBI36
NG_009018.1:g.253037C= , LRG_214:g.253037C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7049C=	ENSP00000512431.1:p.Pro2350=
ENST00000684826.1:c.1631C=	ENSP00000509994.1:p.Pro544=
ENST00000687027.1:c.1223C=	ENSP00000508715.1:p.Pro408=
ENST00000687863.1:n.3712C=
ENST00000689464.1:c.6C=
ENST00000691014.1:c.7097C=	ENSP00000510595.1:p.Pro2366=
ENST00000693617.1:c.1631C=	ENSP00000510031.1:p.Pro544=
ENST00000358273.9:c.7067C= MANE Select	ENSP00000351015.4:p.Pro2356=
ENST00000356175.7:c.7004C=	ENSP00000348498.3:p.Pro2335=
ENST00000358273.8:c.7067C=	ENSP00000351015.4:p.Pro2356=
ENST00000456735.6:c.6002C=	ENSP00000389907.2:p.Pro2001=
ENST00000471572.6:c.450C=
ENST00000579081.5:c.7203C=	ENSP00000462408.1:n.7203C=
ENST00000581790.5:c.210C=
ENST00000582892.1:n.309C=
ENST00000584328.1:n.481C=
NM_000267.3:c.7004C= , LRG_214t1:c.7004C=	NP_000258.1:p.Pro2335=
NM_001042492.2:c.7067C= , LRG_214t2:c.7067C=	NP_001035957.1:p.Pro2356=
XM_005257983.1:c.7067C=	XP_005258040.1:p.Pro2356=
XM_005257984.1:c.7004C=	XP_005258041.1:p.Pro2335=
XM_006721922.1:c.7097C=	XP_006721985.1:p.Pro2366=
XM_006721923.2:c.7058C=	XP_006721986.1:p.Pro2353=
XM_006721924.1:c.7097C=	XP_006721987.1:p.Pro2366=
XM_006721925.1:c.7034C=	XP_006721988.1:p.Pro2345=
XM_006721926.2:c.7097C=	XP_006721989.1:p.Pro2366=
XM_006721927.1:c.7097C=	XP_006721990.1:p.Pro2366=
XM_011524852.1:c.7094C=	XP_011523154.1:p.Pro2365=
XM_011524853.1:c.7058C=	XP_011523155.1:p.Pro2353=
XM_011524854.1:c.7058C=	XP_011523156.1:p.Pro2353=
XM_011524855.1:c.7058C=	XP_011523157.1:p.Pro2353=
XM_011524856.1:c.7058C=	XP_011523158.1:p.Pro2353=
XM_011524857.1:c.7097C=	XP_011523159.1:p.Pro2366=
NM_001042492.3:c.7067C= MANE Select	NP_001035957.1:p.Pro2356=