Canonical Allele Identifier: CA398984229

Gene: NF1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31229152C>T , CM000679.2:g.31229152C>T	GRCh38
NC_000017.10:g.29556170C>T , CM000679.1:g.29556170C>T	GRCh37
NC_000017.9:g.26580296C>T	NCBI36
NG_009018.1:g.139176C>T , LRG_214:g.139176C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.2582C>T	ENSP00000512431.1:p.Ala861Val
ENST00000691014.1:c.2567C>T	ENSP00000510595.1:p.Ala856Val
ENST00000358273.9:c.2537C>T MANE Select	ENSP00000351015.4:p.Ala846Val
ENST00000356175.7:c.2537C>T	ENSP00000348498.3:p.Ala846Val
ENST00000358273.8:c.2537C>T	ENSP00000351015.4:p.Ala846Val
ENST00000456735.6:c.1535C>T	ENSP00000389907.2:p.Ala512Val
ENST00000493220.5:n.704C>T
ENST00000495910.6:c.2312C>T
ENST00000579081.5:c.2639C>T	ENSP00000462408.1:p.Ala880Val
NM_000267.3:c.2537C>T , LRG_214t1:c.2537C>T	NP_000258.1:p.Ala846Val
NM_001042492.2:c.2537C>T , LRG_214t2:c.2537C>T	NP_001035957.1:p.Ala846Val
XM_005257983.1:c.2537C>T	XP_005258040.1:p.Ala846Val
XM_005257984.1:c.2537C>T	XP_005258041.1:p.Ala846Val
XM_006721922.1:c.2567C>T	XP_006721985.1:p.Ala856Val
XM_006721923.2:c.2528C>T	XP_006721986.1:p.Ala843Val
XM_006721924.1:c.2567C>T	XP_006721987.1:p.Ala856Val
XM_006721925.1:c.2567C>T	XP_006721988.1:p.Ala856Val
XM_006721926.2:c.2567C>T	XP_006721989.1:p.Ala856Val
XM_006721927.1:c.2567C>T	XP_006721990.1:p.Ala856Val
XM_006721928.2:c.2567C>T	XP_006721991.1:p.Ala856Val
XM_011524852.1:c.2564C>T	XP_011523154.1:p.Ala855Val
XM_011524853.1:c.2528C>T	XP_011523155.1:p.Ala843Val
XM_011524854.1:c.2528C>T	XP_011523156.1:p.Ala843Val
XM_011524855.1:c.2528C>T	XP_011523157.1:p.Ala843Val
XM_011524856.1:c.2528C>T	XP_011523158.1:p.Ala843Val
XM_011524857.1:c.2567C>T	XP_011523159.1:p.Ala856Val
NM_001042492.3:c.2537C>T MANE Select	NP_001035957.1:p.Ala846Val