Canonical Allele Identifier: CA916080696
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 851908
ClinVar RCV Id: RCV001056416
dbSNP Id: rs1597851420

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31343103_31343104dup , CM000679.2:g.31343103_31343104dup GRCh38
NC_000017.10:g.29670121_29670122dup , CM000679.1:g.29670121_29670122dup GRCh37
NC_000017.9:g.26694247_26694248dup NCBI36
NG_009018.1:g.253127_253128dup , LRG_214:g.253127_253128dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.7139_7140dup ENSP00000512431.1:p.Asn2381LeufsTer10
ENST00000684826.1:c.1721_1722dup ENSP00000509994.1:p.Asn575LeufsTer10
ENST00000687027.1:c.1313_1314dup ENSP00000508715.1:p.Asn439LeufsTer10
ENST00000687863.1:n.3802_3803dup
ENST00000689464.1:c.96_97dup
ENST00000691014.1:c.7187_7188dup ENSP00000510595.1:p.Asn2397LeufsTer10
ENST00000693617.1:c.1721_1722dup ENSP00000510031.1:p.Asn575LeufsTer10
ENST00000358273.9:c.7157_7158dup MANE Select ENSP00000351015.4:p.Asn2387LeufsTer10
ENST00000356175.7:c.7094_7095dup ENSP00000348498.3:p.Asn2366LeufsTer10
ENST00000358273.8:c.7157_7158dup ENSP00000351015.4:p.Asn2387LeufsTer10
ENST00000456735.6:c.6092_6093dup ENSP00000389907.2:p.Asn2032LeufsTer10
ENST00000471572.6:c.540_541dup
ENST00000579081.5:c.7293_7294dup ENSP00000462408.1:n.7293_7294dup
ENST00000581790.5:c.300_301dup
ENST00000582892.1:n.399_400dup
NM_000267.3:c.7094_7095dup , LRG_214t1:c.7094_7095dup NP_000258.1:p.Asn2366LeufsTer10
NM_001042492.2:c.7157_7158dup , LRG_214t2:c.7157_7158dup NP_001035957.1:p.Asn2387LeufsTer10
XM_005257983.1:c.7157_7158dup XP_005258040.1:p.Asn2387LeufsTer10
XM_005257984.1:c.7094_7095dup XP_005258041.1:p.Asn2366LeufsTer10
XM_006721922.1:c.7187_7188dup XP_006721985.1:p.Asn2397LeufsTer10
XM_006721923.2:c.7148_7149dup XP_006721986.1:p.Asn2384LeufsTer10
XM_006721924.1:c.7187_7188dup XP_006721987.1:p.Asn2397LeufsTer10
XM_006721925.1:c.7124_7125dup XP_006721988.1:p.Asn2376LeufsTer10
XM_006721926.2:c.7187_7188dup XP_006721989.1:p.Asn2397LeufsTer10
XM_006721927.1:c.7187_7188dup XP_006721990.1:p.Asn2397LeufsTer10
XM_011524852.1:c.7184_7185dup XP_011523154.1:p.Asn2396LeufsTer10
XM_011524853.1:c.7148_7149dup XP_011523155.1:p.Asn2384LeufsTer10
XM_011524854.1:c.7148_7149dup XP_011523156.1:p.Asn2384LeufsTer10
XM_011524855.1:c.7148_7149dup XP_011523157.1:p.Asn2384LeufsTer10
XM_011524856.1:c.7148_7149dup XP_011523158.1:p.Asn2384LeufsTer10
XM_011524857.1:c.7187_7188dup XP_011523159.1:p.Asn2397LeufsTer10
NM_001042492.3:c.7157_7158dup MANE Select NP_001035957.1:p.Asn2387LeufsTer10