Canonical Allele Identifier: CA399000113
Gene: NF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31261718A>C , CM000679.2:g.31261718A>C GRCh38
NC_000017.10:g.29588736A>C , CM000679.1:g.29588736A>C GRCh37
NC_000017.9:g.26612862A>C NCBI36
NG_009018.1:g.171742A>C , LRG_214:g.171742A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000581113.7:c.387A>C ENSP00000492721.2:p.Ile129=
ENST00000696138.1:c.4567A>C ENSP00000512431.1:p.Lys1523Gln
ENST00000696140.1:n.691A>C
ENST00000696141.1:c.576A>C
ENST00000687863.1:n.1230A>C
ENST00000691014.1:c.4615A>C ENSP00000510595.1:p.Lys1539Gln
ENST00000358273.9:c.4585A>C MANE Select ENSP00000351015.4:p.Lys1529Gln
ENST00000356175.7:c.4522A>C ENSP00000348498.3:p.Lys1508Gln
ENST00000358273.8:c.4585A>C ENSP00000351015.4:p.Lys1529Gln
ENST00000456735.6:c.3520A>C ENSP00000389907.2:p.Lys1174Gln
ENST00000466819.5:c.1101A>C
ENST00000479614.1:c.1038A>C
ENST00000493220.5:n.3058A>C
ENST00000579081.5:c.4624A>C ENSP00000462408.1:p.Lys1542Gln
NM_000267.3:c.4522A>C , LRG_214t1:c.4522A>C NP_000258.1:p.Lys1508Gln
NM_001042492.2:c.4585A>C , LRG_214t2:c.4585A>C NP_001035957.1:p.Lys1529Gln
XM_005257983.1:c.4585A>C XP_005258040.1:p.Lys1529Gln
XM_005257984.1:c.4522A>C XP_005258041.1:p.Lys1508Gln
XM_006721922.1:c.4615A>C XP_006721985.1:p.Lys1539Gln
XM_006721923.2:c.4576A>C XP_006721986.1:p.Lys1526Gln
XM_006721924.1:c.4615A>C XP_006721987.1:p.Lys1539Gln
XM_006721925.1:c.4552A>C XP_006721988.1:p.Lys1518Gln
XM_006721926.2:c.4615A>C XP_006721989.1:p.Lys1539Gln
XM_006721927.1:c.4615A>C XP_006721990.1:p.Lys1539Gln
XM_006721928.2:c.4615A>C XP_006721991.1:p.Lys1539Gln
XM_011524852.1:c.4612A>C XP_011523154.1:p.Lys1538Gln
XM_011524853.1:c.4576A>C XP_011523155.1:p.Lys1526Gln
XM_011524854.1:c.4576A>C XP_011523156.1:p.Lys1526Gln
XM_011524855.1:c.4576A>C XP_011523157.1:p.Lys1526Gln
XM_011524856.1:c.4576A>C XP_011523158.1:p.Lys1526Gln
XM_011524857.1:c.4615A>C XP_011523159.1:p.Lys1539Gln
NM_001042492.3:c.4585A>C MANE Select NP_001035957.1:p.Lys1529Gln