Canonical Allele Identifier: CA399016720
Gene: NF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31349154A>C , CM000679.2:g.31349154A>C GRCh38
NC_000017.10:g.29676172A>C , CM000679.1:g.29676172A>C GRCh37
NC_000017.9:g.26700298A>C NCBI36
NG_009018.1:g.259178A>C , LRG_214:g.259178A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.7206A>C ENSP00000512431.1:p.Arg2402Ser
ENST00000684826.1:c.1788A>C ENSP00000509994.1:p.Arg596Ser
ENST00000687027.1:c.1380A>C ENSP00000508715.1:p.Arg460Ser
ENST00000687863.1:n.3869A>C
ENST00000689464.1:c.274A>C
ENST00000691014.1:c.7254A>C ENSP00000510595.1:p.Arg2418Ser
ENST00000693617.1:c.1788A>C ENSP00000510031.1:p.Arg596Ser
ENST00000358273.9:c.7224A>C MANE Select ENSP00000351015.4:p.Arg2408Ser
ENST00000356175.7:c.7161A>C ENSP00000348498.3:p.Arg2387Ser
ENST00000358273.8:c.7224A>C ENSP00000351015.4:p.Arg2408Ser
ENST00000456735.6:c.6159A>C ENSP00000389907.2:p.Arg2053Ser
ENST00000471572.6:c.607A>C
ENST00000579081.5:c.7360A>C ENSP00000462408.1:n.7360A>C
ENST00000581790.5:c.367A>C
NM_000267.3:c.7161A>C , LRG_214t1:c.7161A>C NP_000258.1:p.Arg2387Ser
NM_001042492.2:c.7224A>C , LRG_214t2:c.7224A>C NP_001035957.1:p.Arg2408Ser
XM_005257983.1:c.7224A>C XP_005258040.1:p.Arg2408Ser
XM_005257984.1:c.7161A>C XP_005258041.1:p.Arg2387Ser
XM_006721922.1:c.7254A>C XP_006721985.1:p.Arg2418Ser
XM_006721923.2:c.7215A>C XP_006721986.1:p.Arg2405Ser
XM_006721924.1:c.7254A>C XP_006721987.1:p.Arg2418Ser
XM_006721925.1:c.7191A>C XP_006721988.1:p.Arg2397Ser
XM_006721926.2:c.7254A>C XP_006721989.1:p.Arg2418Ser
XM_006721927.1:c.7254A>C XP_006721990.1:p.Arg2418Ser
XM_011524852.1:c.7251A>C XP_011523154.1:p.Arg2417Ser
XM_011524853.1:c.7215A>C XP_011523155.1:p.Arg2405Ser
XM_011524854.1:c.7215A>C XP_011523156.1:p.Arg2405Ser
XM_011524855.1:c.7215A>C XP_011523157.1:p.Arg2405Ser
XM_011524856.1:c.7215A>C XP_011523158.1:p.Arg2405Ser
XM_011524857.1:c.7254A>C XP_011523159.1:p.Arg2418Ser
NM_001042492.3:c.7224A>C MANE Select NP_001035957.1:p.Arg2408Ser