Canonical Allele Identifier: CA398997607
Gene: NF1 HGNC NCBI

Linked Data

dbSNP Id: rs2151461840

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31258369A>C , CM000679.2:g.31258369A>C GRCh38
NC_000017.10:g.29585387A>C , CM000679.1:g.29585387A>C GRCh37
NC_000017.9:g.26609513A>C NCBI36
NG_009018.1:g.168393A>C , LRG_214:g.168393A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.4181A>C ENSP00000512431.1:p.Asn1394Thr
ENST00000696140.1:n.305A>C
ENST00000696141.1:c.190A>C
ENST00000687863.1:n.844A>C
ENST00000691014.1:c.4229A>C ENSP00000510595.1:p.Asn1410Thr
ENST00000691649.1:n.171A>C
ENST00000358273.9:c.4199A>C MANE Select ENSP00000351015.4:p.Asn1400Thr
ENST00000356175.7:c.4136A>C ENSP00000348498.3:p.Asn1379Thr
ENST00000358273.8:c.4199A>C ENSP00000351015.4:p.Asn1400Thr
ENST00000456735.6:c.3134A>C ENSP00000389907.2:p.Asn1045Thr
ENST00000466819.5:c.715A>C
ENST00000479614.1:c.652A>C
ENST00000493220.5:n.2672A>C
ENST00000579081.5:c.4238A>C ENSP00000462408.1:p.Asn1413Thr
NM_000267.3:c.4136A>C , LRG_214t1:c.4136A>C NP_000258.1:p.Asn1379Thr
NM_001042492.2:c.4199A>C , LRG_214t2:c.4199A>C NP_001035957.1:p.Asn1400Thr
XM_005257983.1:c.4199A>C XP_005258040.1:p.Asn1400Thr
XM_005257984.1:c.4136A>C XP_005258041.1:p.Asn1379Thr
XM_006721922.1:c.4229A>C XP_006721985.1:p.Asn1410Thr
XM_006721923.2:c.4190A>C XP_006721986.1:p.Asn1397Thr
XM_006721924.1:c.4229A>C XP_006721987.1:p.Asn1410Thr
XM_006721925.1:c.4166A>C XP_006721988.1:p.Asn1389Thr
XM_006721926.2:c.4229A>C XP_006721989.1:p.Asn1410Thr
XM_006721927.1:c.4229A>C XP_006721990.1:p.Asn1410Thr
XM_006721928.2:c.4229A>C XP_006721991.1:p.Asn1410Thr
XM_011524852.1:c.4226A>C XP_011523154.1:p.Asn1409Thr
XM_011524853.1:c.4190A>C XP_011523155.1:p.Asn1397Thr
XM_011524854.1:c.4190A>C XP_011523156.1:p.Asn1397Thr
XM_011524855.1:c.4190A>C XP_011523157.1:p.Asn1397Thr
XM_011524856.1:c.4190A>C XP_011523158.1:p.Asn1397Thr
XM_011524857.1:c.4229A>C XP_011523159.1:p.Asn1410Thr
NM_001042492.3:c.4199A>C MANE Select NP_001035957.1:p.Asn1400Thr