Canonical Allele Identifier: CA398985019

Gene: NF1

Linked Data

• dbSNP Id: rs2151429470
• MyVariant Identifiers: chr17:g.29556332C>A (hg19) ; chr17:g.31229314C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31229314C>A , CM000679.2:g.31229314C>A	GRCh38
NC_000017.10:g.29556332C>A , CM000679.1:g.29556332C>A	GRCh37
NC_000017.9:g.26580458C>A	NCBI36
NG_009018.1:g.139338C>A , LRG_214:g.139338C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696138.1:c.2744C>A	ENSP00000512431.1:p.Ser915Tyr
ENST00000696139.1:c.44C>A	ENSP00000512432.1:p.Ser15Tyr
ENST00000691014.1:c.2729C>A	ENSP00000510595.1:p.Ser910Tyr
ENST00000358273.9:c.2699C>A MANE Select	ENSP00000351015.4:p.Ser900Tyr
ENST00000356175.7:c.2699C>A	ENSP00000348498.3:p.Ser900Tyr
ENST00000358273.8:c.2699C>A	ENSP00000351015.4:p.Ser900Tyr
ENST00000456735.6:c.1697C>A	ENSP00000389907.2:p.Ser566Tyr
ENST00000493220.5:n.866C>A
ENST00000495910.6:c.2474C>A
ENST00000579081.5:c.2801C>A	ENSP00000462408.1:p.Ser934Tyr
NM_000267.3:c.2699C>A , LRG_214t1:c.2699C>A	NP_000258.1:p.Ser900Tyr
NM_001042492.2:c.2699C>A , LRG_214t2:c.2699C>A	NP_001035957.1:p.Ser900Tyr
XM_005257983.1:c.2699C>A	XP_005258040.1:p.Ser900Tyr
XM_005257984.1:c.2699C>A	XP_005258041.1:p.Ser900Tyr
XM_006721922.1:c.2729C>A	XP_006721985.1:p.Ser910Tyr
XM_006721923.2:c.2690C>A	XP_006721986.1:p.Ser897Tyr
XM_006721924.1:c.2729C>A	XP_006721987.1:p.Ser910Tyr
XM_006721925.1:c.2729C>A	XP_006721988.1:p.Ser910Tyr
XM_006721926.2:c.2729C>A	XP_006721989.1:p.Ser910Tyr
XM_006721927.1:c.2729C>A	XP_006721990.1:p.Ser910Tyr
XM_006721928.2:c.2729C>A	XP_006721991.1:p.Ser910Tyr
XM_011524852.1:c.2726C>A	XP_011523154.1:p.Ser909Tyr
XM_011524853.1:c.2690C>A	XP_011523155.1:p.Ser897Tyr
XM_011524854.1:c.2690C>A	XP_011523156.1:p.Ser897Tyr
XM_011524855.1:c.2690C>A	XP_011523157.1:p.Ser897Tyr
XM_011524856.1:c.2690C>A	XP_011523158.1:p.Ser897Tyr
XM_011524857.1:c.2729C>A	XP_011523159.1:p.Ser910Tyr
NM_001042492.3:c.2699C>A MANE Select	NP_001035957.1:p.Ser900Tyr