Canonical Allele Identifier: CA2255615058

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31357269G= , CM000679.2:g.31357269G=	GRCh38
NC_000017.10:g.29684287G= , CM000679.1:g.29684287G=	GRCh37
NC_000017.9:g.26708413G=	NCBI36
NG_009018.1:g.267293G= , LRG_214:g.267293G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7852G=	ENSP00000512431.1:p.Ala2618=
ENST00000684826.1:c.2434G=	ENSP00000509994.1:p.Ala812=
ENST00000687027.1:c.2026G=	ENSP00000508715.1:p.Ala676=
ENST00000687863.1:n.4515G=
ENST00000689464.1:c.920G=
ENST00000691014.1:c.7900G=	ENSP00000510595.1:p.Ala2634=
ENST00000693617.1:c.2434G=	ENSP00000510031.1:p.Ala812=
ENST00000358273.9:c.7870G= MANE Select	ENSP00000351015.4:p.Ala2624=
ENST00000356175.7:c.7807G=	ENSP00000348498.3:p.Ala2603=
ENST00000358273.8:c.7870G=	ENSP00000351015.4:p.Ala2624=
ENST00000456735.6:c.6805G=	ENSP00000389907.2:p.Ala2269=
ENST00000471572.6:c.1253G=
ENST00000577967.1:n.1466G=
ENST00000579081.5:c.8006G=	ENSP00000462408.1:n.8006G=
ENST00000581790.5:c.855G=
NM_000267.3:c.7807G= , LRG_214t1:c.7807G=	NP_000258.1:p.Ala2603=
NM_001042492.2:c.7870G= , LRG_214t2:c.7870G=	NP_001035957.1:p.Ala2624=
XM_005257983.1:c.7870G=	XP_005258040.1:p.Ala2624=
XM_005257984.1:c.7807G=	XP_005258041.1:p.Ala2603=
XM_006721922.1:c.7900G=	XP_006721985.1:p.Ala2634=
XM_006721923.2:c.7861G=	XP_006721986.1:p.Ala2621=
XM_006721924.1:c.7900G=	XP_006721987.1:p.Ala2634=
XM_006721925.1:c.7837G=	XP_006721988.1:p.Ala2613=
XM_006721926.2:c.7900G=	XP_006721989.1:p.Ala2634=
XM_006721927.1:c.7900G=	XP_006721990.1:p.Ala2634=
XM_011524852.1:c.7897G=	XP_011523154.1:p.Ala2633=
XM_011524853.1:c.7861G=	XP_011523155.1:p.Ala2621=
XM_011524854.1:c.7861G=	XP_011523156.1:p.Ala2621=
XM_011524855.1:c.7861G=	XP_011523157.1:p.Ala2621=
XM_011524856.1:c.7861G=	XP_011523158.1:p.Ala2621=
XM_011524857.1:c.7777G=	XP_011523159.1:p.Ala2593=
NM_001042492.3:c.7870G= MANE Select	NP_001035957.1:p.Ala2624=