Canonical Allele Identifier: CA398986390

Gene: NF1

Linked Data

• ClinVar Variation Id: 941469
• ClinVar RCV Id: RCV001211258
• dbSNP Id: rs1060500298
• MyVariant Identifiers: chr17:g.29556974T>G (hg19) ; chr17:g.31229956T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31229956T>G , CM000679.2:g.31229956T>G	GRCh38
NC_000017.10:g.29556974T>G , CM000679.1:g.29556974T>G	GRCh37
NC_000017.9:g.26581100T>G	NCBI36
NG_009018.1:g.139980T>G , LRG_214:g.139980T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.3017T>G	ENSP00000512431.1:p.Met1006Arg
ENST00000696139.1:c.317T>G	ENSP00000512432.1:p.Met106Arg
ENST00000691014.1:c.3002T>G	ENSP00000510595.1:p.Met1001Arg
ENST00000358273.9:c.2972T>G MANE Select	ENSP00000351015.4:p.Met991Arg
ENST00000356175.7:c.2972T>G	ENSP00000348498.3:p.Met991Arg
ENST00000358273.8:c.2972T>G	ENSP00000351015.4:p.Met991Arg
ENST00000456735.6:c.1970T>G	ENSP00000389907.2:p.Met657Arg
ENST00000493220.5:n.1508T>G
ENST00000495910.6:c.2747T>G
ENST00000579081.5:c.3074T>G	ENSP00000462408.1:p.Met1025Arg
NM_000267.3:c.2972T>G , LRG_214t1:c.2972T>G	NP_000258.1:p.Met991Arg
NM_001042492.2:c.2972T>G , LRG_214t2:c.2972T>G	NP_001035957.1:p.Met991Arg
XM_005257983.1:c.2972T>G	XP_005258040.1:p.Met991Arg
XM_005257984.1:c.2972T>G	XP_005258041.1:p.Met991Arg
XM_006721922.1:c.3002T>G	XP_006721985.1:p.Met1001Arg
XM_006721923.2:c.2963T>G	XP_006721986.1:p.Met988Arg
XM_006721924.1:c.3002T>G	XP_006721987.1:p.Met1001Arg
XM_006721925.1:c.3002T>G	XP_006721988.1:p.Met1001Arg
XM_006721926.2:c.3002T>G	XP_006721989.1:p.Met1001Arg
XM_006721927.1:c.3002T>G	XP_006721990.1:p.Met1001Arg
XM_006721928.2:c.3002T>G	XP_006721991.1:p.Met1001Arg
XM_011524852.1:c.2999T>G	XP_011523154.1:p.Met1000Arg
XM_011524853.1:c.2963T>G	XP_011523155.1:p.Met988Arg
XM_011524854.1:c.2963T>G	XP_011523156.1:p.Met988Arg
XM_011524855.1:c.2963T>G	XP_011523157.1:p.Met988Arg
XM_011524856.1:c.2963T>G	XP_011523158.1:p.Met988Arg
XM_011524857.1:c.3002T>G	XP_011523159.1:p.Met1001Arg
NM_001042492.3:c.2972T>G MANE Select	NP_001035957.1:p.Met991Arg