Canonical Allele Identifier: CA399015655

Gene: NF1

Linked Data

• MyVariant Identifiers: chr17:g.29670093T>G (hg19) ; chr17:g.31343075T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31343075T>G , CM000679.2:g.31343075T>G	GRCh38
NC_000017.10:g.29670093T>G , CM000679.1:g.29670093T>G	GRCh37
NC_000017.9:g.26694219T>G	NCBI36
NG_009018.1:g.253099T>G , LRG_214:g.253099T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7111T>G	ENSP00000512431.1:p.Phe2371Val
ENST00000684826.1:c.1693T>G	ENSP00000509994.1:p.Phe565Val
ENST00000687027.1:c.1285T>G	ENSP00000508715.1:p.Phe429Val
ENST00000687863.1:n.3774T>G
ENST00000689464.1:c.68T>G
ENST00000691014.1:c.7159T>G	ENSP00000510595.1:p.Phe2387Val
ENST00000693617.1:c.1693T>G	ENSP00000510031.1:p.Phe565Val
ENST00000358273.9:c.7129T>G MANE Select	ENSP00000351015.4:p.Phe2377Val
ENST00000356175.7:c.7066T>G	ENSP00000348498.3:p.Phe2356Val
ENST00000358273.8:c.7129T>G	ENSP00000351015.4:p.Phe2377Val
ENST00000456735.6:c.6064T>G	ENSP00000389907.2:p.Phe2022Val
ENST00000471572.6:c.512T>G
ENST00000579081.5:c.7265T>G	ENSP00000462408.1:n.7265T>G
ENST00000581790.5:c.272T>G
ENST00000582892.1:n.371T>G
ENST00000584328.1:n.543T>G
NM_000267.3:c.7066T>G , LRG_214t1:c.7066T>G	NP_000258.1:p.Phe2356Val
NM_001042492.2:c.7129T>G , LRG_214t2:c.7129T>G	NP_001035957.1:p.Phe2377Val
XM_005257983.1:c.7129T>G	XP_005258040.1:p.Phe2377Val
XM_005257984.1:c.7066T>G	XP_005258041.1:p.Phe2356Val
XM_006721922.1:c.7159T>G	XP_006721985.1:p.Phe2387Val
XM_006721923.2:c.7120T>G	XP_006721986.1:p.Phe2374Val
XM_006721924.1:c.7159T>G	XP_006721987.1:p.Phe2387Val
XM_006721925.1:c.7096T>G	XP_006721988.1:p.Phe2366Val
XM_006721926.2:c.7159T>G	XP_006721989.1:p.Phe2387Val
XM_006721927.1:c.7159T>G	XP_006721990.1:p.Phe2387Val
XM_011524852.1:c.7156T>G	XP_011523154.1:p.Phe2386Val
XM_011524853.1:c.7120T>G	XP_011523155.1:p.Phe2374Val
XM_011524854.1:c.7120T>G	XP_011523156.1:p.Phe2374Val
XM_011524855.1:c.7120T>G	XP_011523157.1:p.Phe2374Val
XM_011524856.1:c.7120T>G	XP_011523158.1:p.Phe2374Val
XM_011524857.1:c.7159T>G	XP_011523159.1:p.Phe2387Val
NM_001042492.3:c.7129T>G MANE Select	NP_001035957.1:p.Phe2377Val