Canonical Allele Identifier: CA399014310

Gene: NF1

Linked Data

• MyVariant Identifiers: chr17:g.29665753C>G (hg19) ; chr17:g.31338735C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31338735C>G , CM000679.2:g.31338735C>G	GRCh38
NC_000017.10:g.29665753C>G , CM000679.1:g.29665753C>G	GRCh37
NC_000017.9:g.26689879C>G	NCBI36
NG_009018.1:g.248759C>G , LRG_214:g.248759C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.6833C>G	ENSP00000512431.1:p.Thr2278Ser
ENST00000684826.1:c.1415C>G	ENSP00000509994.1:p.Thr472Ser
ENST00000684998.1:n.2673C>G
ENST00000687027.1:c.1007C>G	ENSP00000508715.1:p.Thr336Ser
ENST00000687863.1:n.3496C>G
ENST00000691014.1:c.6881C>G	ENSP00000510595.1:p.Thr2294Ser
ENST00000693617.1:c.1415C>G	ENSP00000510031.1:p.Thr472Ser
ENST00000358273.9:c.6851C>G MANE Select	ENSP00000351015.4:p.Thr2284Ser
ENST00000356175.7:c.6788C>G	ENSP00000348498.3:p.Thr2263Ser
ENST00000358273.8:c.6851C>G	ENSP00000351015.4:p.Thr2284Ser
ENST00000456735.6:c.5786C>G	ENSP00000389907.2:p.Thr1929Ser
ENST00000471572.6:c.234C>G
ENST00000579081.5:c.6987C>G	ENSP00000462408.1:n.6987C>G
ENST00000581790.5:c.64+855C>G
ENST00000584328.1:n.265C>G
NM_000267.3:c.6788C>G , LRG_214t1:c.6788C>G	NP_000258.1:p.Thr2263Ser
NM_001042492.2:c.6851C>G , LRG_214t2:c.6851C>G	NP_001035957.1:p.Thr2284Ser
XM_005257983.1:c.6851C>G	XP_005258040.1:p.Thr2284Ser
XM_005257984.1:c.6788C>G	XP_005258041.1:p.Thr2263Ser
XM_006721922.1:c.6881C>G	XP_006721985.1:p.Thr2294Ser
XM_006721923.2:c.6842C>G	XP_006721986.1:p.Thr2281Ser
XM_006721924.1:c.6881C>G	XP_006721987.1:p.Thr2294Ser
XM_006721925.1:c.6818C>G	XP_006721988.1:p.Thr2273Ser
XM_006721926.2:c.6881C>G	XP_006721989.1:p.Thr2294Ser
XM_006721927.1:c.6881C>G	XP_006721990.1:p.Thr2294Ser
XM_011524852.1:c.6878C>G	XP_011523154.1:p.Thr2293Ser
XM_011524853.1:c.6842C>G	XP_011523155.1:p.Thr2281Ser
XM_011524854.1:c.6842C>G	XP_011523156.1:p.Thr2281Ser
XM_011524855.1:c.6842C>G	XP_011523157.1:p.Thr2281Ser
XM_011524856.1:c.6842C>G	XP_011523158.1:p.Thr2281Ser
XM_011524857.1:c.6881C>G	XP_011523159.1:p.Thr2294Ser
NM_001042492.3:c.6851C>G MANE Select	NP_001035957.1:p.Thr2284Ser