Canonical Allele Identifier: CA399015712

Gene: NF1

Linked Data

• MyVariant Identifiers: chr17:g.29670119C>A (hg19) ; chr17:g.31343101C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31343101C>A , CM000679.2:g.31343101C>A	GRCh38
NC_000017.10:g.29670119C>A , CM000679.1:g.29670119C>A	GRCh37
NC_000017.9:g.26694245C>A	NCBI36
NG_009018.1:g.253125C>A , LRG_214:g.253125C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7137C>A	ENSP00000512431.1:p.Asn2379Lys
ENST00000684826.1:c.1719C>A	ENSP00000509994.1:p.Asn573Lys
ENST00000687027.1:c.1311C>A	ENSP00000508715.1:p.Asn437Lys
ENST00000687863.1:n.3800C>A
ENST00000689464.1:c.94C>A
ENST00000691014.1:c.7185C>A	ENSP00000510595.1:p.Asn2395Lys
ENST00000693617.1:c.1719C>A	ENSP00000510031.1:p.Asn573Lys
ENST00000358273.9:c.7155C>A MANE Select	ENSP00000351015.4:p.Asn2385Lys
ENST00000356175.7:c.7092C>A	ENSP00000348498.3:p.Asn2364Lys
ENST00000358273.8:c.7155C>A	ENSP00000351015.4:p.Asn2385Lys
ENST00000456735.6:c.6090C>A	ENSP00000389907.2:p.Asn2030Lys
ENST00000471572.6:c.538C>A
ENST00000579081.5:c.7291C>A	ENSP00000462408.1:n.7291C>A
ENST00000581790.5:c.298C>A
ENST00000582892.1:n.397C>A
NM_000267.3:c.7092C>A , LRG_214t1:c.7092C>A	NP_000258.1:p.Asn2364Lys
NM_001042492.2:c.7155C>A , LRG_214t2:c.7155C>A	NP_001035957.1:p.Asn2385Lys
XM_005257983.1:c.7155C>A	XP_005258040.1:p.Asn2385Lys
XM_005257984.1:c.7092C>A	XP_005258041.1:p.Asn2364Lys
XM_006721922.1:c.7185C>A	XP_006721985.1:p.Asn2395Lys
XM_006721923.2:c.7146C>A	XP_006721986.1:p.Asn2382Lys
XM_006721924.1:c.7185C>A	XP_006721987.1:p.Asn2395Lys
XM_006721925.1:c.7122C>A	XP_006721988.1:p.Asn2374Lys
XM_006721926.2:c.7185C>A	XP_006721989.1:p.Asn2395Lys
XM_006721927.1:c.7185C>A	XP_006721990.1:p.Asn2395Lys
XM_011524852.1:c.7182C>A	XP_011523154.1:p.Asn2394Lys
XM_011524853.1:c.7146C>A	XP_011523155.1:p.Asn2382Lys
XM_011524854.1:c.7146C>A	XP_011523156.1:p.Asn2382Lys
XM_011524855.1:c.7146C>A	XP_011523157.1:p.Asn2382Lys
XM_011524856.1:c.7146C>A	XP_011523158.1:p.Asn2382Lys
XM_011524857.1:c.7185C>A	XP_011523159.1:p.Asn2395Lys
NM_001042492.3:c.7155C>A MANE Select	NP_001035957.1:p.Asn2385Lys