Canonical Allele Identifier: CA399000082

Gene: NF1

Linked Data

• dbSNP Id: rs1356757316
• MyVariant Identifiers: chr17:g.29588729G>C (hg19) ; chr17:g.31261711G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31261711G>C , CM000679.2:g.31261711G>C	GRCh38
NC_000017.10:g.29588729G>C , CM000679.1:g.29588729G>C	GRCh37
NC_000017.9:g.26612855G>C	NCBI36
NG_009018.1:g.171735G>C , LRG_214:g.171735G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000581113.7:c.380G>C	ENSP00000492721.2:p.Gly127Ala
ENST00000696138.1:c.4560G>C	ENSP00000512431.1:p.Arg1520Ser
ENST00000696140.1:n.684G>C
ENST00000696141.1:c.569G>C
ENST00000687863.1:n.1223G>C
ENST00000691014.1:c.4608G>C	ENSP00000510595.1:p.Arg1536Ser
ENST00000358273.9:c.4578G>C MANE Select	ENSP00000351015.4:p.Arg1526Ser
ENST00000356175.7:c.4515G>C	ENSP00000348498.3:p.Arg1505Ser
ENST00000358273.8:c.4578G>C	ENSP00000351015.4:p.Arg1526Ser
ENST00000456735.6:c.3513G>C	ENSP00000389907.2:p.Arg1171Ser
ENST00000466819.5:c.1094G>C
ENST00000479614.1:c.1031G>C
ENST00000493220.5:n.3051G>C
ENST00000579081.5:c.4617G>C	ENSP00000462408.1:p.Arg1539Ser
NM_000267.3:c.4515G>C , LRG_214t1:c.4515G>C	NP_000258.1:p.Arg1505Ser
NM_001042492.2:c.4578G>C , LRG_214t2:c.4578G>C	NP_001035957.1:p.Arg1526Ser
XM_005257983.1:c.4578G>C	XP_005258040.1:p.Arg1526Ser
XM_005257984.1:c.4515G>C	XP_005258041.1:p.Arg1505Ser
XM_006721922.1:c.4608G>C	XP_006721985.1:p.Arg1536Ser
XM_006721923.2:c.4569G>C	XP_006721986.1:p.Arg1523Ser
XM_006721924.1:c.4608G>C	XP_006721987.1:p.Arg1536Ser
XM_006721925.1:c.4545G>C	XP_006721988.1:p.Arg1515Ser
XM_006721926.2:c.4608G>C	XP_006721989.1:p.Arg1536Ser
XM_006721927.1:c.4608G>C	XP_006721990.1:p.Arg1536Ser
XM_006721928.2:c.4608G>C	XP_006721991.1:p.Arg1536Ser
XM_011524852.1:c.4605G>C	XP_011523154.1:p.Arg1535Ser
XM_011524853.1:c.4569G>C	XP_011523155.1:p.Arg1523Ser
XM_011524854.1:c.4569G>C	XP_011523156.1:p.Arg1523Ser
XM_011524855.1:c.4569G>C	XP_011523157.1:p.Arg1523Ser
XM_011524856.1:c.4569G>C	XP_011523158.1:p.Arg1523Ser
XM_011524857.1:c.4608G>C	XP_011523159.1:p.Arg1536Ser
NM_001042492.3:c.4578G>C MANE Select	NP_001035957.1:p.Arg1526Ser