Canonical Allele Identifier: CA399001352

Gene: NF1

Linked Data

• MyVariant Identifiers: chr17:g.29592338T>G (hg19) ; chr17:g.31265320T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31265320T>G , CM000679.2:g.31265320T>G	GRCh38
NC_000017.10:g.29592338T>G , CM000679.1:g.29592338T>G	GRCh37
NC_000017.9:g.26616464T>G	NCBI36
NG_009018.1:g.175344T>G , LRG_214:g.175344T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581113.7:c.618T>G	ENSP00000492721.2:n.618T>G
ENST00000696138.1:c.4798T>G	ENSP00000512431.1:p.Phe1600Val
ENST00000696140.1:n.922T>G
ENST00000696141.1:c.807T>G
ENST00000687863.1:n.1461T>G
ENST00000691014.1:c.4846T>G	ENSP00000510595.1:p.Phe1616Val
ENST00000358273.9:c.4816T>G MANE Select	ENSP00000351015.4:p.Phe1606Val
ENST00000356175.7:c.4753T>G	ENSP00000348498.3:p.Phe1585Val
ENST00000358273.8:c.4816T>G	ENSP00000351015.4:p.Phe1606Val
ENST00000456735.6:c.3751T>G	ENSP00000389907.2:p.Phe1251Val
ENST00000493220.5:n.3289T>G
ENST00000579081.5:c.4855T>G	ENSP00000462408.1:p.Phe1619Val
NM_000267.3:c.4753T>G , LRG_214t1:c.4753T>G	NP_000258.1:p.Phe1585Val
NM_001042492.2:c.4816T>G , LRG_214t2:c.4816T>G	NP_001035957.1:p.Phe1606Val
XM_005257983.1:c.4816T>G	XP_005258040.1:p.Phe1606Val
XM_005257984.1:c.4753T>G	XP_005258041.1:p.Phe1585Val
XM_006721922.1:c.4846T>G	XP_006721985.1:p.Phe1616Val
XM_006721923.2:c.4807T>G	XP_006721986.1:p.Phe1603Val
XM_006721924.1:c.4846T>G	XP_006721987.1:p.Phe1616Val
XM_006721925.1:c.4783T>G	XP_006721988.1:p.Phe1595Val
XM_006721926.2:c.4846T>G	XP_006721989.1:p.Phe1616Val
XM_006721927.1:c.4846T>G	XP_006721990.1:p.Phe1616Val
XM_006721928.2:c.4846T>G	XP_006721991.1:p.Phe1616Val
XM_011524852.1:c.4843T>G	XP_011523154.1:p.Phe1615Val
XM_011524853.1:c.4807T>G	XP_011523155.1:p.Phe1603Val
XM_011524854.1:c.4807T>G	XP_011523156.1:p.Phe1603Val
XM_011524855.1:c.4807T>G	XP_011523157.1:p.Phe1603Val
XM_011524856.1:c.4807T>G	XP_011523158.1:p.Phe1603Val
XM_011524857.1:c.4846T>G	XP_011523159.1:p.Phe1616Val
NM_001042492.3:c.4816T>G MANE Select	NP_001035957.1:p.Phe1606Val