Canonical Allele Identifier: CA398984245

Gene: NF1

Linked Data

• dbSNP Id: rs1064794275
• MyVariant Identifiers: chr17:g.29556178G>A (hg19) ; chr17:g.31229160G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31229160G>A , CM000679.2:g.31229160G>A	GRCh38
NC_000017.10:g.29556178G>A , CM000679.1:g.29556178G>A	GRCh37
NC_000017.9:g.26580304G>A	NCBI36
NG_009018.1:g.139184G>A , LRG_214:g.139184G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696138.1:c.2590G>A	ENSP00000512431.1:p.Gly864Arg
ENST00000691014.1:c.2575G>A	ENSP00000510595.1:p.Gly859Arg
ENST00000358273.9:c.2545G>A MANE Select	ENSP00000351015.4:p.Gly849Arg
ENST00000356175.7:c.2545G>A	ENSP00000348498.3:p.Gly849Arg
ENST00000358273.8:c.2545G>A	ENSP00000351015.4:p.Gly849Arg
ENST00000456735.6:c.1543G>A	ENSP00000389907.2:p.Gly515Arg
ENST00000493220.5:n.712G>A
ENST00000495910.6:c.2320G>A
ENST00000579081.5:c.2647G>A	ENSP00000462408.1:p.Gly883Arg
NM_000267.3:c.2545G>A , LRG_214t1:c.2545G>A	NP_000258.1:p.Gly849Arg
NM_001042492.2:c.2545G>A , LRG_214t2:c.2545G>A	NP_001035957.1:p.Gly849Arg
XM_005257983.1:c.2545G>A	XP_005258040.1:p.Gly849Arg
XM_005257984.1:c.2545G>A	XP_005258041.1:p.Gly849Arg
XM_006721922.1:c.2575G>A	XP_006721985.1:p.Gly859Arg
XM_006721923.2:c.2536G>A	XP_006721986.1:p.Gly846Arg
XM_006721924.1:c.2575G>A	XP_006721987.1:p.Gly859Arg
XM_006721925.1:c.2575G>A	XP_006721988.1:p.Gly859Arg
XM_006721926.2:c.2575G>A	XP_006721989.1:p.Gly859Arg
XM_006721927.1:c.2575G>A	XP_006721990.1:p.Gly859Arg
XM_006721928.2:c.2575G>A	XP_006721991.1:p.Gly859Arg
XM_011524852.1:c.2572G>A	XP_011523154.1:p.Gly858Arg
XM_011524853.1:c.2536G>A	XP_011523155.1:p.Gly846Arg
XM_011524854.1:c.2536G>A	XP_011523156.1:p.Gly846Arg
XM_011524855.1:c.2536G>A	XP_011523157.1:p.Gly846Arg
XM_011524856.1:c.2536G>A	XP_011523158.1:p.Gly846Arg
XM_011524857.1:c.2575G>A	XP_011523159.1:p.Gly859Arg
NM_001042492.3:c.2545G>A MANE Select	NP_001035957.1:p.Gly849Arg