Canonical Allele Identifier: CA2255617596

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31330475G= , CM000679.2:g.31330475G=	GRCh38
NC_000017.10:g.29657493G= , CM000679.1:g.29657493G=	GRCh37
NC_000017.9:g.26681619G=	NCBI36
NG_009018.1:g.240499G= , LRG_214:g.240499G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581113.7:c.1977G=	ENSP00000492721.2:n.1977G=
ENST00000696138.1:c.5771G=	ENSP00000512431.1:p.Cys1924=
ENST00000684826.1:c.353G=	ENSP00000509994.1:p.Cys118=
ENST00000687027.1:c.-56G=	ENSP00000508715.1:n.-56G=
ENST00000687863.1:n.2434G=
ENST00000691014.1:c.5819G=	ENSP00000510595.1:p.Cys1940=
ENST00000693617.1:c.353G=	ENSP00000510031.1:p.Cys118=
ENST00000358273.9:c.5789G= MANE Select	ENSP00000351015.4:p.Cys1930=
ENST00000356175.7:c.5726G=	ENSP00000348498.3:p.Cys1909=
ENST00000358273.8:c.5789G=	ENSP00000351015.4:p.Cys1930=
ENST00000456735.6:c.4724G=	ENSP00000389907.2:p.Cys1575=
ENST00000479536.2:c.147G=
ENST00000493220.5:n.4262G=
ENST00000579081.5:c.5925G=	ENSP00000462408.1:n.5925G=
ENST00000581113.6:n.1106G=
NM_000267.3:c.5726G= , LRG_214t1:c.5726G=	NP_000258.1:p.Cys1909=
NM_001042492.2:c.5789G= , LRG_214t2:c.5789G=	NP_001035957.1:p.Cys1930=
XM_005257983.1:c.5789G=	XP_005258040.1:p.Cys1930=
XM_005257984.1:c.5726G=	XP_005258041.1:p.Cys1909=
XM_006721922.1:c.5819G=	XP_006721985.1:p.Cys1940=
XM_006721923.2:c.5780G=	XP_006721986.1:p.Cys1927=
XM_006721924.1:c.5819G=	XP_006721987.1:p.Cys1940=
XM_006721925.1:c.5756G=	XP_006721988.1:p.Cys1919=
XM_006721926.2:c.5819G=	XP_006721989.1:p.Cys1940=
XM_006721927.1:c.5819G=	XP_006721990.1:p.Cys1940=
XM_011524852.1:c.5816G=	XP_011523154.1:p.Cys1939=
XM_011524853.1:c.5780G=	XP_011523155.1:p.Cys1927=
XM_011524854.1:c.5780G=	XP_011523156.1:p.Cys1927=
XM_011524855.1:c.5780G=	XP_011523157.1:p.Cys1927=
XM_011524856.1:c.5780G=	XP_011523158.1:p.Cys1927=
XM_011524857.1:c.5819G=	XP_011523159.1:p.Cys1940=
NM_001042492.3:c.5789G= MANE Select	NP_001035957.1:p.Cys1930=