Canonical Allele Identifier: CA399015505

Gene: NF1

Linked Data

• ClinVar Variation Id: 2167054
• ClinVar RCV Id: RCV003098937
• dbSNP Id: rs1567620376
• MyVariant Identifiers: chr17:g.29670029T>A (hg19) ; chr17:g.31343011T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31343011T>A , CM000679.2:g.31343011T>A	GRCh38
NC_000017.10:g.29670029T>A , CM000679.1:g.29670029T>A	GRCh37
NC_000017.9:g.26694155T>A	NCBI36
NG_009018.1:g.253035T>A , LRG_214:g.253035T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7047T>A	ENSP00000512431.1:p.Ser2349Arg
ENST00000684826.1:c.1629T>A	ENSP00000509994.1:p.Ser543Arg
ENST00000687027.1:c.1221T>A	ENSP00000508715.1:p.Ser407Arg
ENST00000687863.1:n.3710T>A
ENST00000689464.1:c.4T>A
ENST00000691014.1:c.7095T>A	ENSP00000510595.1:p.Ser2365Arg
ENST00000693617.1:c.1629T>A	ENSP00000510031.1:p.Ser543Arg
ENST00000358273.9:c.7065T>A MANE Select	ENSP00000351015.4:p.Ser2355Arg
ENST00000356175.7:c.7002T>A	ENSP00000348498.3:p.Ser2334Arg
ENST00000358273.8:c.7065T>A	ENSP00000351015.4:p.Ser2355Arg
ENST00000456735.6:c.6000T>A	ENSP00000389907.2:p.Ser2000Arg
ENST00000471572.6:c.448T>A
ENST00000579081.5:c.7201T>A	ENSP00000462408.1:n.7201T>A
ENST00000581790.5:c.208T>A
ENST00000582892.1:n.307T>A
ENST00000584328.1:n.479T>A
NM_000267.3:c.7002T>A , LRG_214t1:c.7002T>A	NP_000258.1:p.Ser2334Arg
NM_001042492.2:c.7065T>A , LRG_214t2:c.7065T>A	NP_001035957.1:p.Ser2355Arg
XM_005257983.1:c.7065T>A	XP_005258040.1:p.Ser2355Arg
XM_005257984.1:c.7002T>A	XP_005258041.1:p.Ser2334Arg
XM_006721922.1:c.7095T>A	XP_006721985.1:p.Ser2365Arg
XM_006721923.2:c.7056T>A	XP_006721986.1:p.Ser2352Arg
XM_006721924.1:c.7095T>A	XP_006721987.1:p.Ser2365Arg
XM_006721925.1:c.7032T>A	XP_006721988.1:p.Ser2344Arg
XM_006721926.2:c.7095T>A	XP_006721989.1:p.Ser2365Arg
XM_006721927.1:c.7095T>A	XP_006721990.1:p.Ser2365Arg
XM_011524852.1:c.7092T>A	XP_011523154.1:p.Ser2364Arg
XM_011524853.1:c.7056T>A	XP_011523155.1:p.Ser2352Arg
XM_011524854.1:c.7056T>A	XP_011523156.1:p.Ser2352Arg
XM_011524855.1:c.7056T>A	XP_011523157.1:p.Ser2352Arg
XM_011524856.1:c.7056T>A	XP_011523158.1:p.Ser2352Arg
XM_011524857.1:c.7095T>A	XP_011523159.1:p.Ser2365Arg
NM_001042492.3:c.7065T>A MANE Select	NP_001035957.1:p.Ser2355Arg