Canonical Allele Identifier: CA8486234

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31235713A>G , CM000679.2:g.31235713A>G	GRCh38
NC_000017.10:g.29562731A>G , CM000679.1:g.29562731A>G	GRCh37
NC_000017.9:g.26586857A>G	NCBI36
NG_009018.1:g.145737A>G , LRG_214:g.145737A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001042492.3:c.3811A>G MANE Select	NP_001035957.1:p.Met1271Val
ENST00000358273.9:c.3811A>G MANE Select	ENSP00000351015.4:p.Met1271Val
NM_000267.3:c.3811A>G , LRG_214t1:c.3811A>G	NP_000258.1:p.Met1271Val
NM_001042492.2:c.3811A>G , LRG_214t2:c.3811A>G	NP_001035957.1:p.Met1271Val
ENST00000356175.7:c.3811A>G	ENSP00000348498.3:p.Met1271Val
ENST00000358273.8:c.3811A>G	ENSP00000351015.4:p.Met1271Val
ENST00000456735.6:c.2809A>G	ENSP00000389907.2:p.Met937Val
ENST00000466819.5:c.287A>G
ENST00000479614.1:c.287A>G
ENST00000493220.5:n.2347A>G
ENST00000495910.6:c.3586A>G
ENST00000579081.5:c.3913A>G	ENSP00000462408.1:p.Met1305Val
ENST00000687863.1:n.519A>G
ENST00000691014.1:c.3841A>G	ENSP00000510595.1:p.Met1281Val
ENST00000696138.1:c.3856A>G	ENSP00000512431.1:p.Met1286Val
ENST00000696139.1:c.1156A>G	ENSP00000512432.1:p.Met386Val
XM_005257983.1:c.3811A>G	XP_005258040.1:p.Met1271Val
XM_005257984.1:c.3811A>G	XP_005258041.1:p.Met1271Val
XM_006721922.1:c.3841A>G	XP_006721985.1:p.Met1281Val
XM_006721923.2:c.3802A>G	XP_006721986.1:p.Met1268Val
XM_006721924.1:c.3841A>G	XP_006721987.1:p.Met1281Val
XM_006721925.1:c.3841A>G	XP_006721988.1:p.Met1281Val
XM_006721926.2:c.3841A>G	XP_006721989.1:p.Met1281Val
XM_006721927.1:c.3841A>G	XP_006721990.1:p.Met1281Val
XM_006721928.2:c.3841A>G	XP_006721991.1:p.Met1281Val
XM_011524852.1:c.3838A>G	XP_011523154.1:p.Met1280Val
XM_011524853.1:c.3802A>G	XP_011523155.1:p.Met1268Val
XM_011524854.1:c.3802A>G	XP_011523156.1:p.Met1268Val
XM_011524855.1:c.3802A>G	XP_011523157.1:p.Met1268Val
XM_011524856.1:c.3802A>G	XP_011523158.1:p.Met1268Val
XM_011524857.1:c.3841A>G	XP_011523159.1:p.Met1281Val