Canonical Allele Identifier: CA891843818

Gene: NF1

Linked Data

• ClinVar Variation Id: 573205
• ClinVar RCV Id: RCV000694813
• dbSNP Id: rs1567851445
• MyVariant Identifiers: chr17:g.29560180dup (hg19) ; chr17:g.31233162dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31233162dup , CM000679.2:g.31233162dup	GRCh38
NC_000017.10:g.29560180dup , CM000679.1:g.29560180dup	GRCh37
NC_000017.9:g.26584306dup	NCBI36
NG_009018.1:g.143186dup , LRG_214:g.143186dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.3702dup	ENSP00000512431.1:p.Glu1235ArgfsTer19
ENST00000696139.1:c.1002dup	ENSP00000512432.1:p.Glu335ArgfsTer19
ENST00000691014.1:c.3687dup	ENSP00000510595.1:p.Glu1230ArgfsTer19
ENST00000693210.1:n.383dup
ENST00000358273.9:c.3657dup MANE Select	ENSP00000351015.4:p.Glu1220ArgfsTer19
ENST00000356175.7:c.3657dup	ENSP00000348498.3:p.Glu1220ArgfsTer19
ENST00000358273.8:c.3657dup	ENSP00000351015.4:p.Glu1220ArgfsTer19
ENST00000456735.6:c.2655dup	ENSP00000389907.2:p.Glu886ArgfsTer19
ENST00000466819.5:c.133dup
ENST00000479614.1:c.133dup
ENST00000493220.5:n.2193dup
ENST00000495910.6:c.3432dup
ENST00000579081.5:c.3759dup	ENSP00000462408.1:p.Glu1254ArgfsTer19
NM_000267.3:c.3657dup , LRG_214t1:c.3657dup	NP_000258.1:p.Glu1220ArgfsTer19
NM_001042492.2:c.3657dup , LRG_214t2:c.3657dup	NP_001035957.1:p.Glu1220ArgfsTer19
XM_005257983.1:c.3657dup	XP_005258040.1:p.Glu1220ArgfsTer19
XM_005257984.1:c.3657dup	XP_005258041.1:p.Glu1220ArgfsTer19
XM_006721922.1:c.3687dup	XP_006721985.1:p.Glu1230ArgfsTer19
XM_006721923.2:c.3648dup	XP_006721986.1:p.Glu1217ArgfsTer19
XM_006721924.1:c.3687dup	XP_006721987.1:p.Glu1230ArgfsTer19
XM_006721925.1:c.3687dup	XP_006721988.1:p.Glu1230ArgfsTer19
XM_006721926.2:c.3687dup	XP_006721989.1:p.Glu1230ArgfsTer19
XM_006721927.1:c.3687dup	XP_006721990.1:p.Glu1230ArgfsTer19
XM_006721928.2:c.3687dup	XP_006721991.1:p.Glu1230ArgfsTer19
XM_011524852.1:c.3684dup	XP_011523154.1:p.Glu1229ArgfsTer19
XM_011524853.1:c.3648dup	XP_011523155.1:p.Glu1217ArgfsTer19
XM_011524854.1:c.3648dup	XP_011523156.1:p.Glu1217ArgfsTer19
XM_011524855.1:c.3648dup	XP_011523157.1:p.Glu1217ArgfsTer19
XM_011524856.1:c.3648dup	XP_011523158.1:p.Glu1217ArgfsTer19
XM_011524857.1:c.3687dup	XP_011523159.1:p.Glu1230ArgfsTer19
NM_001042492.3:c.3657dup MANE Select	NP_001035957.1:p.Glu1220ArgfsTer19