Canonical Allele Identifier: CA499234376

Gene: NF1

Linked Data

• MyVariant Identifiers: chr17:g.29665811A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31338793A>G , CM000679.2:g.31338793A>G	GRCh38
NC_000017.10:g.29665811A>G , CM000679.1:g.29665811A>G	GRCh37
NC_000017.9:g.26689937A>G	NCBI36
NG_009018.1:g.248817A>G , LRG_214:g.248817A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.6891A>G	ENSP00000512431.1:p.Pro2297=
ENST00000684826.1:c.1473A>G	ENSP00000509994.1:p.Pro491=
ENST00000684998.1:n.2731A>G
ENST00000687027.1:c.1065A>G	ENSP00000508715.1:p.Pro355=
ENST00000687863.1:n.3554A>G
ENST00000691014.1:c.6939A>G	ENSP00000510595.1:p.Pro2313=
ENST00000693617.1:c.1473A>G	ENSP00000510031.1:p.Pro491=
ENST00000358273.9:c.6909A>G MANE Select	ENSP00000351015.4:p.Pro2303=
ENST00000356175.7:c.6846A>G	ENSP00000348498.3:p.Pro2282=
ENST00000358273.8:c.6909A>G	ENSP00000351015.4:p.Pro2303=
ENST00000456735.6:c.5844A>G	ENSP00000389907.2:p.Pro1948=
ENST00000471572.6:c.292A>G
ENST00000579081.5:c.7045A>G	ENSP00000462408.1:n.7045A>G
ENST00000581790.5:c.64+913A>G
ENST00000584328.1:n.323A>G
NM_000267.3:c.6846A>G , LRG_214t1:c.6846A>G	NP_000258.1:p.Pro2282=
NM_001042492.2:c.6909A>G , LRG_214t2:c.6909A>G	NP_001035957.1:p.Pro2303=
XM_005257983.1:c.6909A>G	XP_005258040.1:p.Pro2303=
XM_005257984.1:c.6846A>G	XP_005258041.1:p.Pro2282=
XM_006721922.1:c.6939A>G	XP_006721985.1:p.Pro2313=
XM_006721923.2:c.6900A>G	XP_006721986.1:p.Pro2300=
XM_006721924.1:c.6939A>G	XP_006721987.1:p.Pro2313=
XM_006721925.1:c.6876A>G	XP_006721988.1:p.Pro2292=
XM_006721926.2:c.6939A>G	XP_006721989.1:p.Pro2313=
XM_006721927.1:c.6939A>G	XP_006721990.1:p.Pro2313=
XM_011524852.1:c.6936A>G	XP_011523154.1:p.Pro2312=
XM_011524853.1:c.6900A>G	XP_011523155.1:p.Pro2300=
XM_011524854.1:c.6900A>G	XP_011523156.1:p.Pro2300=
XM_011524855.1:c.6900A>G	XP_011523157.1:p.Pro2300=
XM_011524856.1:c.6900A>G	XP_011523158.1:p.Pro2300=
XM_011524857.1:c.6939A>G	XP_011523159.1:p.Pro2313=
NM_001042492.3:c.6909A>G MANE Select	NP_001035957.1:p.Pro2303=