Canonical Allele Identifier: CA399015517

Gene: NF1

Linked Data

• dbSNP Id: rs1368077280
• MyVariant Identifiers: chr17:g.29670035G>C (hg19) ; chr17:g.31343017G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31343017G>C , CM000679.2:g.31343017G>C	GRCh38
NC_000017.10:g.29670035G>C , CM000679.1:g.29670035G>C	GRCh37
NC_000017.9:g.26694161G>C	NCBI36
NG_009018.1:g.253041G>C , LRG_214:g.253041G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7053G>C	ENSP00000512431.1:p.Glu2351Asp
ENST00000684826.1:c.1635G>C	ENSP00000509994.1:p.Glu545Asp
ENST00000687027.1:c.1227G>C	ENSP00000508715.1:p.Glu409Asp
ENST00000687863.1:n.3716G>C
ENST00000689464.1:c.10G>C
ENST00000691014.1:c.7101G>C	ENSP00000510595.1:p.Glu2367Asp
ENST00000693617.1:c.1635G>C	ENSP00000510031.1:p.Glu545Asp
ENST00000358273.9:c.7071G>C MANE Select	ENSP00000351015.4:p.Glu2357Asp
ENST00000356175.7:c.7008G>C	ENSP00000348498.3:p.Glu2336Asp
ENST00000358273.8:c.7071G>C	ENSP00000351015.4:p.Glu2357Asp
ENST00000456735.6:c.6006G>C	ENSP00000389907.2:p.Glu2002Asp
ENST00000471572.6:c.454G>C
ENST00000579081.5:c.7207G>C	ENSP00000462408.1:n.7207G>C
ENST00000581790.5:c.214G>C
ENST00000582892.1:n.313G>C
ENST00000584328.1:n.485G>C
NM_000267.3:c.7008G>C , LRG_214t1:c.7008G>C	NP_000258.1:p.Glu2336Asp
NM_001042492.2:c.7071G>C , LRG_214t2:c.7071G>C	NP_001035957.1:p.Glu2357Asp
XM_005257983.1:c.7071G>C	XP_005258040.1:p.Glu2357Asp
XM_005257984.1:c.7008G>C	XP_005258041.1:p.Glu2336Asp
XM_006721922.1:c.7101G>C	XP_006721985.1:p.Glu2367Asp
XM_006721923.2:c.7062G>C	XP_006721986.1:p.Glu2354Asp
XM_006721924.1:c.7101G>C	XP_006721987.1:p.Glu2367Asp
XM_006721925.1:c.7038G>C	XP_006721988.1:p.Glu2346Asp
XM_006721926.2:c.7101G>C	XP_006721989.1:p.Glu2367Asp
XM_006721927.1:c.7101G>C	XP_006721990.1:p.Glu2367Asp
XM_011524852.1:c.7098G>C	XP_011523154.1:p.Glu2366Asp
XM_011524853.1:c.7062G>C	XP_011523155.1:p.Glu2354Asp
XM_011524854.1:c.7062G>C	XP_011523156.1:p.Glu2354Asp
XM_011524855.1:c.7062G>C	XP_011523157.1:p.Glu2354Asp
XM_011524856.1:c.7062G>C	XP_011523158.1:p.Glu2354Asp
XM_011524857.1:c.7101G>C	XP_011523159.1:p.Glu2367Asp
NM_001042492.3:c.7071G>C MANE Select	NP_001035957.1:p.Glu2357Asp