Canonical Allele Identifier: CA399014277
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2862745
ClinVar RCV Id: RCV003597556

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31338720T>G , CM000679.2:g.31338720T>G GRCh38
NC_000017.10:g.29665738T>G , CM000679.1:g.29665738T>G GRCh37
NC_000017.9:g.26689864T>G NCBI36
NG_009018.1:g.248744T>G , LRG_214:g.248744T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.6818T>G ENSP00000512431.1:p.Leu2273Ter
ENST00000684826.1:c.1400T>G ENSP00000509994.1:p.Leu467Ter
ENST00000684998.1:n.2658T>G
ENST00000687027.1:c.992T>G ENSP00000508715.1:p.Leu331Ter
ENST00000687863.1:n.3481T>G
ENST00000691014.1:c.6866T>G ENSP00000510595.1:p.Leu2289Ter
ENST00000693617.1:c.1400T>G ENSP00000510031.1:p.Leu467Ter
ENST00000358273.9:c.6836T>G MANE Select ENSP00000351015.4:p.Leu2279Ter
ENST00000356175.7:c.6773T>G ENSP00000348498.3:p.Leu2258Ter
ENST00000358273.8:c.6836T>G ENSP00000351015.4:p.Leu2279Ter
ENST00000456735.6:c.5771T>G ENSP00000389907.2:p.Leu1924Ter
ENST00000471572.6:c.219T>G
ENST00000579081.5:c.6972T>G ENSP00000462408.1:n.6972T>G
ENST00000581790.5:c.64+840T>G
ENST00000584328.1:n.250T>G
NM_000267.3:c.6773T>G , LRG_214t1:c.6773T>G NP_000258.1:p.Leu2258Ter
NM_001042492.2:c.6836T>G , LRG_214t2:c.6836T>G NP_001035957.1:p.Leu2279Ter
XM_005257983.1:c.6836T>G XP_005258040.1:p.Leu2279Ter
XM_005257984.1:c.6773T>G XP_005258041.1:p.Leu2258Ter
XM_006721922.1:c.6866T>G XP_006721985.1:p.Leu2289Ter
XM_006721923.2:c.6827T>G XP_006721986.1:p.Leu2276Ter
XM_006721924.1:c.6866T>G XP_006721987.1:p.Leu2289Ter
XM_006721925.1:c.6803T>G XP_006721988.1:p.Leu2268Ter
XM_006721926.2:c.6866T>G XP_006721989.1:p.Leu2289Ter
XM_006721927.1:c.6866T>G XP_006721990.1:p.Leu2289Ter
XM_011524852.1:c.6863T>G XP_011523154.1:p.Leu2288Ter
XM_011524853.1:c.6827T>G XP_011523155.1:p.Leu2276Ter
XM_011524854.1:c.6827T>G XP_011523156.1:p.Leu2276Ter
XM_011524855.1:c.6827T>G XP_011523157.1:p.Leu2276Ter
XM_011524856.1:c.6827T>G XP_011523158.1:p.Leu2276Ter
XM_011524857.1:c.6866T>G XP_011523159.1:p.Leu2289Ter
NM_001042492.3:c.6836T>G MANE Select NP_001035957.1:p.Leu2279Ter