Canonical Allele Identifier: CA8486127

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31232117C>G , CM000679.2:g.31232117C>G	GRCh38
NC_000017.10:g.29559135C>G , CM000679.1:g.29559135C>G	GRCh37
NC_000017.9:g.26583261C>G	NCBI36
NG_009018.1:g.142141C>G , LRG_214:g.142141C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001042492.3:c.3242C>G MANE Select	NP_001035957.1:p.Ala1081Gly
ENST00000358273.9:c.3242C>G MANE Select	ENSP00000351015.4:p.Ala1081Gly
NM_000267.3:c.3242C>G , LRG_214t1:c.3242C>G	NP_000258.1:p.Ala1081Gly
NM_001042492.2:c.3242C>G , LRG_214t2:c.3242C>G	NP_001035957.1:p.Ala1081Gly
ENST00000356175.7:c.3242C>G	ENSP00000348498.3:p.Ala1081Gly
ENST00000358273.8:c.3242C>G	ENSP00000351015.4:p.Ala1081Gly
ENST00000456735.6:c.2240C>G	ENSP00000389907.2:p.Ala747Gly
ENST00000493220.5:n.1778C>G
ENST00000495910.6:c.3017C>G
ENST00000579081.5:c.3344C>G	ENSP00000462408.1:p.Ala1115Gly
ENST00000691014.1:c.3272C>G	ENSP00000510595.1:p.Ala1091Gly
ENST00000696138.1:c.3287C>G	ENSP00000512431.1:p.Ala1096Gly
ENST00000696139.1:c.587C>G	ENSP00000512432.1:p.Ala196Gly
XM_005257983.1:c.3242C>G	XP_005258040.1:p.Ala1081Gly
XM_005257984.1:c.3242C>G	XP_005258041.1:p.Ala1081Gly
XM_006721922.1:c.3272C>G	XP_006721985.1:p.Ala1091Gly
XM_006721923.2:c.3233C>G	XP_006721986.1:p.Ala1078Gly
XM_006721924.1:c.3272C>G	XP_006721987.1:p.Ala1091Gly
XM_006721925.1:c.3272C>G	XP_006721988.1:p.Ala1091Gly
XM_006721926.2:c.3272C>G	XP_006721989.1:p.Ala1091Gly
XM_006721927.1:c.3272C>G	XP_006721990.1:p.Ala1091Gly
XM_006721928.2:c.3272C>G	XP_006721991.1:p.Ala1091Gly
XM_011524852.1:c.3269C>G	XP_011523154.1:p.Ala1090Gly
XM_011524853.1:c.3233C>G	XP_011523155.1:p.Ala1078Gly
XM_011524854.1:c.3233C>G	XP_011523156.1:p.Ala1078Gly
XM_011524855.1:c.3233C>G	XP_011523157.1:p.Ala1078Gly
XM_011524856.1:c.3233C>G	XP_011523158.1:p.Ala1078Gly
XM_011524857.1:c.3272C>G	XP_011523159.1:p.Ala1091Gly