Canonical Allele Identifier: CA398999872
Gene: NF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31260496C>A , CM000679.2:g.31260496C>A GRCh38
NC_000017.10:g.29587514C>A , CM000679.1:g.29587514C>A GRCh37
NC_000017.9:g.26611640C>A NCBI36
NG_009018.1:g.170520C>A , LRG_214:g.170520C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000581113.7:c.346C>A ENSP00000492721.2:p.Gln116Lys
ENST00000696138.1:c.4540C>A ENSP00000512431.1:p.Gln1514Lys
ENST00000696140.1:n.664C>A
ENST00000696141.1:c.549C>A
ENST00000687863.1:n.1203C>A
ENST00000691014.1:c.4588C>A ENSP00000510595.1:p.Gln1530Lys
ENST00000691649.1:n.1769C>A
ENST00000358273.9:c.4558C>A MANE Select ENSP00000351015.4:p.Gln1520Lys
ENST00000356175.7:c.4495C>A ENSP00000348498.3:p.Gln1499Lys
ENST00000358273.8:c.4558C>A ENSP00000351015.4:p.Gln1520Lys
ENST00000456735.6:c.3493C>A ENSP00000389907.2:p.Gln1165Lys
ENST00000466819.5:c.1074C>A
ENST00000479614.1:c.1011C>A
ENST00000493220.5:n.3031C>A
ENST00000579081.5:c.4597C>A ENSP00000462408.1:p.Gln1533Lys
NM_000267.3:c.4495C>A , LRG_214t1:c.4495C>A NP_000258.1:p.Gln1499Lys
NM_001042492.2:c.4558C>A , LRG_214t2:c.4558C>A NP_001035957.1:p.Gln1520Lys
XM_005257983.1:c.4558C>A XP_005258040.1:p.Gln1520Lys
XM_005257984.1:c.4495C>A XP_005258041.1:p.Gln1499Lys
XM_006721922.1:c.4588C>A XP_006721985.1:p.Gln1530Lys
XM_006721923.2:c.4549C>A XP_006721986.1:p.Gln1517Lys
XM_006721924.1:c.4588C>A XP_006721987.1:p.Gln1530Lys
XM_006721925.1:c.4525C>A XP_006721988.1:p.Gln1509Lys
XM_006721926.2:c.4588C>A XP_006721989.1:p.Gln1530Lys
XM_006721927.1:c.4588C>A XP_006721990.1:p.Gln1530Lys
XM_006721928.2:c.4588C>A XP_006721991.1:p.Gln1530Lys
XM_011524852.1:c.4585C>A XP_011523154.1:p.Gln1529Lys
XM_011524853.1:c.4549C>A XP_011523155.1:p.Gln1517Lys
XM_011524854.1:c.4549C>A XP_011523156.1:p.Gln1517Lys
XM_011524855.1:c.4549C>A XP_011523157.1:p.Gln1517Lys
XM_011524856.1:c.4549C>A XP_011523158.1:p.Gln1517Lys
XM_011524857.1:c.4588C>A XP_011523159.1:p.Gln1530Lys
NM_001042492.3:c.4558C>A MANE Select NP_001035957.1:p.Gln1520Lys