Canonical Allele Identifier: CA398984570

Gene: NF1

Linked Data

• ClinVar Variation Id: 821610
• ClinVar RCV Id: RCV002319249 ; RCV002549435
• dbSNP Id: rs1597715515
• MyVariant Identifiers: chr17:g.29556264G>T (hg19) ; chr17:g.31229246G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31229246G>T , CM000679.2:g.31229246G>T	GRCh38
NC_000017.10:g.29556264G>T , CM000679.1:g.29556264G>T	GRCh37
NC_000017.9:g.26580390G>T	NCBI36
NG_009018.1:g.139270G>T , LRG_214:g.139270G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.2676G>T	ENSP00000512431.1:p.Met892Ile
ENST00000691014.1:c.2661G>T	ENSP00000510595.1:p.Met887Ile
ENST00000358273.9:c.2631G>T MANE Select	ENSP00000351015.4:p.Met877Ile
ENST00000356175.7:c.2631G>T	ENSP00000348498.3:p.Met877Ile
ENST00000358273.8:c.2631G>T	ENSP00000351015.4:p.Met877Ile
ENST00000456735.6:c.1629G>T	ENSP00000389907.2:p.Met543Ile
ENST00000493220.5:n.798G>T
ENST00000495910.6:c.2406G>T
ENST00000579081.5:c.2733G>T	ENSP00000462408.1:p.Met911Ile
NM_000267.3:c.2631G>T , LRG_214t1:c.2631G>T	NP_000258.1:p.Met877Ile
NM_001042492.2:c.2631G>T , LRG_214t2:c.2631G>T	NP_001035957.1:p.Met877Ile
XM_005257983.1:c.2631G>T	XP_005258040.1:p.Met877Ile
XM_005257984.1:c.2631G>T	XP_005258041.1:p.Met877Ile
XM_006721922.1:c.2661G>T	XP_006721985.1:p.Met887Ile
XM_006721923.2:c.2622G>T	XP_006721986.1:p.Met874Ile
XM_006721924.1:c.2661G>T	XP_006721987.1:p.Met887Ile
XM_006721925.1:c.2661G>T	XP_006721988.1:p.Met887Ile
XM_006721926.2:c.2661G>T	XP_006721989.1:p.Met887Ile
XM_006721927.1:c.2661G>T	XP_006721990.1:p.Met887Ile
XM_006721928.2:c.2661G>T	XP_006721991.1:p.Met887Ile
XM_011524852.1:c.2658G>T	XP_011523154.1:p.Met886Ile
XM_011524853.1:c.2622G>T	XP_011523155.1:p.Met874Ile
XM_011524854.1:c.2622G>T	XP_011523156.1:p.Met874Ile
XM_011524855.1:c.2622G>T	XP_011523157.1:p.Met874Ile
XM_011524856.1:c.2622G>T	XP_011523158.1:p.Met874Ile
XM_011524857.1:c.2661G>T	XP_011523159.1:p.Met887Ile
NM_001042492.3:c.2631G>T MANE Select	NP_001035957.1:p.Met877Ile