Canonical Allele Identifier: CA399001269
Gene: NF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31265282T>C , CM000679.2:g.31265282T>C GRCh38
NC_000017.10:g.29592300T>C , CM000679.1:g.29592300T>C GRCh37
NC_000017.9:g.26616426T>C NCBI36
NG_009018.1:g.175306T>C , LRG_214:g.175306T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000581113.7:c.580T>C ENSP00000492721.2:n.580T>C
ENST00000696138.1:c.4760T>C ENSP00000512431.1:p.Phe1587Ser
ENST00000696140.1:n.884T>C
ENST00000696141.1:c.769T>C
ENST00000687863.1:n.1423T>C
ENST00000691014.1:c.4808T>C ENSP00000510595.1:p.Phe1603Ser
ENST00000358273.9:c.4778T>C MANE Select ENSP00000351015.4:p.Phe1593Ser
ENST00000356175.7:c.4715T>C ENSP00000348498.3:p.Phe1572Ser
ENST00000358273.8:c.4778T>C ENSP00000351015.4:p.Phe1593Ser
ENST00000456735.6:c.3713T>C ENSP00000389907.2:p.Phe1238Ser
ENST00000493220.5:n.3251T>C
ENST00000579081.5:c.4817T>C ENSP00000462408.1:p.Phe1606Ser
NM_000267.3:c.4715T>C , LRG_214t1:c.4715T>C NP_000258.1:p.Phe1572Ser
NM_001042492.2:c.4778T>C , LRG_214t2:c.4778T>C NP_001035957.1:p.Phe1593Ser
XM_005257983.1:c.4778T>C XP_005258040.1:p.Phe1593Ser
XM_005257984.1:c.4715T>C XP_005258041.1:p.Phe1572Ser
XM_006721922.1:c.4808T>C XP_006721985.1:p.Phe1603Ser
XM_006721923.2:c.4769T>C XP_006721986.1:p.Phe1590Ser
XM_006721924.1:c.4808T>C XP_006721987.1:p.Phe1603Ser
XM_006721925.1:c.4745T>C XP_006721988.1:p.Phe1582Ser
XM_006721926.2:c.4808T>C XP_006721989.1:p.Phe1603Ser
XM_006721927.1:c.4808T>C XP_006721990.1:p.Phe1603Ser
XM_006721928.2:c.4808T>C XP_006721991.1:p.Phe1603Ser
XM_011524852.1:c.4805T>C XP_011523154.1:p.Phe1602Ser
XM_011524853.1:c.4769T>C XP_011523155.1:p.Phe1590Ser
XM_011524854.1:c.4769T>C XP_011523156.1:p.Phe1590Ser
XM_011524855.1:c.4769T>C XP_011523157.1:p.Phe1590Ser
XM_011524856.1:c.4769T>C XP_011523158.1:p.Phe1590Ser
XM_011524857.1:c.4808T>C XP_011523159.1:p.Phe1603Ser
NM_001042492.3:c.4778T>C MANE Select NP_001035957.1:p.Phe1593Ser