Canonical Allele Identifier: CA399000407
Gene: NF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31261794T>A , CM000679.2:g.31261794T>A GRCh38
NC_000017.10:g.29588812T>A , CM000679.1:g.29588812T>A GRCh37
NC_000017.9:g.26612938T>A NCBI36
NG_009018.1:g.171818T>A , LRG_214:g.171818T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000581113.7:c.463T>A ENSP00000492721.2:p.Trp155Arg
ENST00000696138.1:c.4643T>A ENSP00000512431.1:p.Val1548Glu
ENST00000696140.1:n.767T>A
ENST00000696141.1:c.652T>A
ENST00000687863.1:n.1306T>A
ENST00000691014.1:c.4691T>A ENSP00000510595.1:p.Val1564Glu
ENST00000358273.9:c.4661T>A MANE Select ENSP00000351015.4:p.Val1554Glu
ENST00000356175.7:c.4598T>A ENSP00000348498.3:p.Val1533Glu
ENST00000358273.8:c.4661T>A ENSP00000351015.4:p.Val1554Glu
ENST00000456735.6:c.3596T>A ENSP00000389907.2:p.Val1199Glu
ENST00000466819.5:c.1177T>A
ENST00000479614.1:c.1114T>A
ENST00000493220.5:n.3134T>A
ENST00000579081.5:c.4700T>A ENSP00000462408.1:p.Val1567Glu
NM_000267.3:c.4598T>A , LRG_214t1:c.4598T>A NP_000258.1:p.Val1533Glu
NM_001042492.2:c.4661T>A , LRG_214t2:c.4661T>A NP_001035957.1:p.Val1554Glu
XM_005257983.1:c.4661T>A XP_005258040.1:p.Val1554Glu
XM_005257984.1:c.4598T>A XP_005258041.1:p.Val1533Glu
XM_006721922.1:c.4691T>A XP_006721985.1:p.Val1564Glu
XM_006721923.2:c.4652T>A XP_006721986.1:p.Val1551Glu
XM_006721924.1:c.4691T>A XP_006721987.1:p.Val1564Glu
XM_006721925.1:c.4628T>A XP_006721988.1:p.Val1543Glu
XM_006721926.2:c.4691T>A XP_006721989.1:p.Val1564Glu
XM_006721927.1:c.4691T>A XP_006721990.1:p.Val1564Glu
XM_006721928.2:c.4691T>A XP_006721991.1:p.Val1564Glu
XM_011524852.1:c.4688T>A XP_011523154.1:p.Val1563Glu
XM_011524853.1:c.4652T>A XP_011523155.1:p.Val1551Glu
XM_011524854.1:c.4652T>A XP_011523156.1:p.Val1551Glu
XM_011524855.1:c.4652T>A XP_011523157.1:p.Val1551Glu
XM_011524856.1:c.4652T>A XP_011523158.1:p.Val1551Glu
XM_011524857.1:c.4691T>A XP_011523159.1:p.Val1564Glu
NM_001042492.3:c.4661T>A MANE Select NP_001035957.1:p.Val1554Glu