Canonical Allele Identifier: CA399000462

Gene: NF1

Linked Data

• ClinVar Variation Id: 825042
• ClinVar RCV Id: RCV002319361 ; RCV003598035
• dbSNP Id: rs1597748910
• gnomAD v4: 17-31261806-A-G
• MyVariant Identifiers: chr17:g.29588824A>G (hg19) ; chr17:g.31261806A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31261806A>G , CM000679.2:g.31261806A>G	GRCh38
NC_000017.10:g.29588824A>G , CM000679.1:g.29588824A>G	GRCh37
NC_000017.9:g.26612950A>G	NCBI36
NG_009018.1:g.171830A>G , LRG_214:g.171830A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581113.7:c.475A>G	ENSP00000492721.2:p.Thr159Ala
ENST00000696138.1:c.4655A>G	ENSP00000512431.1:p.His1552Arg
ENST00000696140.1:n.779A>G
ENST00000696141.1:c.664A>G
ENST00000687863.1:n.1318A>G
ENST00000691014.1:c.4703A>G	ENSP00000510595.1:p.His1568Arg
ENST00000358273.9:c.4673A>G MANE Select	ENSP00000351015.4:p.His1558Arg
ENST00000356175.7:c.4610A>G	ENSP00000348498.3:p.His1537Arg
ENST00000358273.8:c.4673A>G	ENSP00000351015.4:p.His1558Arg
ENST00000456735.6:c.3608A>G	ENSP00000389907.2:p.His1203Arg
ENST00000493220.5:n.3146A>G
ENST00000579081.5:c.4712A>G	ENSP00000462408.1:p.His1571Arg
NM_000267.3:c.4610A>G , LRG_214t1:c.4610A>G	NP_000258.1:p.His1537Arg
NM_001042492.2:c.4673A>G , LRG_214t2:c.4673A>G	NP_001035957.1:p.His1558Arg
XM_005257983.1:c.4673A>G	XP_005258040.1:p.His1558Arg
XM_005257984.1:c.4610A>G	XP_005258041.1:p.His1537Arg
XM_006721922.1:c.4703A>G	XP_006721985.1:p.His1568Arg
XM_006721923.2:c.4664A>G	XP_006721986.1:p.His1555Arg
XM_006721924.1:c.4703A>G	XP_006721987.1:p.His1568Arg
XM_006721925.1:c.4640A>G	XP_006721988.1:p.His1547Arg
XM_006721926.2:c.4703A>G	XP_006721989.1:p.His1568Arg
XM_006721927.1:c.4703A>G	XP_006721990.1:p.His1568Arg
XM_006721928.2:c.4703A>G	XP_006721991.1:p.His1568Arg
XM_011524852.1:c.4700A>G	XP_011523154.1:p.His1567Arg
XM_011524853.1:c.4664A>G	XP_011523155.1:p.His1555Arg
XM_011524854.1:c.4664A>G	XP_011523156.1:p.His1555Arg
XM_011524855.1:c.4664A>G	XP_011523157.1:p.His1555Arg
XM_011524856.1:c.4664A>G	XP_011523158.1:p.His1555Arg
XM_011524857.1:c.4703A>G	XP_011523159.1:p.His1568Arg
NM_001042492.3:c.4673A>G MANE Select	NP_001035957.1:p.His1558Arg