Canonical Allele Identifier: CA2255607709

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31349147T= , CM000679.2:g.31349147T=	GRCh38
NC_000017.10:g.29676165T= , CM000679.1:g.29676165T=	GRCh37
NC_000017.9:g.26700291T=	NCBI36
NG_009018.1:g.259171T= , LRG_214:g.259171T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7199T=	ENSP00000512431.1:p.Val2400=
ENST00000684826.1:c.1781T=	ENSP00000509994.1:p.Val594=
ENST00000687027.1:c.1373T=	ENSP00000508715.1:p.Val458=
ENST00000687863.1:n.3862T=
ENST00000689464.1:c.267T=
ENST00000691014.1:c.7247T=	ENSP00000510595.1:p.Val2416=
ENST00000693617.1:c.1781T=	ENSP00000510031.1:p.Val594=
ENST00000358273.9:c.7217T= MANE Select	ENSP00000351015.4:p.Val2406=
ENST00000356175.7:c.7154T=	ENSP00000348498.3:p.Val2385=
ENST00000358273.8:c.7217T=	ENSP00000351015.4:p.Val2406=
ENST00000456735.6:c.6152T=	ENSP00000389907.2:p.Val2051=
ENST00000471572.6:c.600T=
ENST00000579081.5:c.7353T=	ENSP00000462408.1:n.7353T=
ENST00000581790.5:c.360T=
ENST00000582892.1:n.459T=
NM_000267.3:c.7154T= , LRG_214t1:c.7154T=	NP_000258.1:p.Val2385=
NM_001042492.2:c.7217T= , LRG_214t2:c.7217T=	NP_001035957.1:p.Val2406=
XM_005257983.1:c.7217T=	XP_005258040.1:p.Val2406=
XM_005257984.1:c.7154T=	XP_005258041.1:p.Val2385=
XM_006721922.1:c.7247T=	XP_006721985.1:p.Val2416=
XM_006721923.2:c.7208T=	XP_006721986.1:p.Val2403=
XM_006721924.1:c.7247T=	XP_006721987.1:p.Val2416=
XM_006721925.1:c.7184T=	XP_006721988.1:p.Val2395=
XM_006721926.2:c.7247T=	XP_006721989.1:p.Val2416=
XM_006721927.1:c.7247T=	XP_006721990.1:p.Val2416=
XM_011524852.1:c.7244T=	XP_011523154.1:p.Val2415=
XM_011524853.1:c.7208T=	XP_011523155.1:p.Val2403=
XM_011524854.1:c.7208T=	XP_011523156.1:p.Val2403=
XM_011524855.1:c.7208T=	XP_011523157.1:p.Val2403=
XM_011524856.1:c.7208T=	XP_011523158.1:p.Val2403=
XM_011524857.1:c.7247T=	XP_011523159.1:p.Val2416=
NM_001042492.3:c.7217T= MANE Select	NP_001035957.1:p.Val2406=