Canonical Allele Identifier: CA399014332

Gene: NF1

Linked Data

• ClinVar Variation Id: 1009231
• ClinVar RCV Id: RCV001306687
• dbSNP Id: rs2069744324
• MyVariant Identifiers: chr17:g.29665763T>G (hg19) ; chr17:g.31338745T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31338745T>G , CM000679.2:g.31338745T>G	GRCh38
NC_000017.10:g.29665763T>G , CM000679.1:g.29665763T>G	GRCh37
NC_000017.9:g.26689889T>G	NCBI36
NG_009018.1:g.248769T>G , LRG_214:g.248769T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.6843T>G	ENSP00000512431.1:p.Ser2281Arg
ENST00000684826.1:c.1425T>G	ENSP00000509994.1:p.Ser475Arg
ENST00000684998.1:n.2683T>G
ENST00000687027.1:c.1017T>G	ENSP00000508715.1:p.Ser339Arg
ENST00000687863.1:n.3506T>G
ENST00000691014.1:c.6891T>G	ENSP00000510595.1:p.Ser2297Arg
ENST00000693617.1:c.1425T>G	ENSP00000510031.1:p.Ser475Arg
ENST00000358273.9:c.6861T>G MANE Select	ENSP00000351015.4:p.Ser2287Arg
ENST00000356175.7:c.6798T>G	ENSP00000348498.3:p.Ser2266Arg
ENST00000358273.8:c.6861T>G	ENSP00000351015.4:p.Ser2287Arg
ENST00000456735.6:c.5796T>G	ENSP00000389907.2:p.Ser1932Arg
ENST00000471572.6:c.244T>G
ENST00000579081.5:c.6997T>G	ENSP00000462408.1:n.6997T>G
ENST00000581790.5:c.64+865T>G
ENST00000584328.1:n.275T>G
NM_000267.3:c.6798T>G , LRG_214t1:c.6798T>G	NP_000258.1:p.Ser2266Arg
NM_001042492.2:c.6861T>G , LRG_214t2:c.6861T>G	NP_001035957.1:p.Ser2287Arg
XM_005257983.1:c.6861T>G	XP_005258040.1:p.Ser2287Arg
XM_005257984.1:c.6798T>G	XP_005258041.1:p.Ser2266Arg
XM_006721922.1:c.6891T>G	XP_006721985.1:p.Ser2297Arg
XM_006721923.2:c.6852T>G	XP_006721986.1:p.Ser2284Arg
XM_006721924.1:c.6891T>G	XP_006721987.1:p.Ser2297Arg
XM_006721925.1:c.6828T>G	XP_006721988.1:p.Ser2276Arg
XM_006721926.2:c.6891T>G	XP_006721989.1:p.Ser2297Arg
XM_006721927.1:c.6891T>G	XP_006721990.1:p.Ser2297Arg
XM_011524852.1:c.6888T>G	XP_011523154.1:p.Ser2296Arg
XM_011524853.1:c.6852T>G	XP_011523155.1:p.Ser2284Arg
XM_011524854.1:c.6852T>G	XP_011523156.1:p.Ser2284Arg
XM_011524855.1:c.6852T>G	XP_011523157.1:p.Ser2284Arg
XM_011524856.1:c.6852T>G	XP_011523158.1:p.Ser2284Arg
XM_011524857.1:c.6891T>G	XP_011523159.1:p.Ser2297Arg
NM_001042492.3:c.6861T>G MANE Select	NP_001035957.1:p.Ser2287Arg