Canonical Allele Identifier: CA399003995

Gene: NF1

Linked Data

• ClinVar Variation Id: 2106645
• ClinVar RCV Id: RCV003026576
• dbSNP Id: rs2144015654
• MyVariant Identifiers: chr17:g.29550471G>A (hg19) ; chr17:g.31223453G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31223453G>A , CM000679.2:g.31223453G>A	GRCh38
NC_000017.10:g.29550471G>A , CM000679.1:g.29550471G>A	GRCh37
NC_000017.9:g.26574597G>A	NCBI36
NG_009018.1:g.133477G>A , LRG_214:g.133477G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696138.1:c.1776G>A	ENSP00000512431.1:p.Met592Ile
ENST00000691014.1:c.1761G>A	ENSP00000510595.1:p.Met587Ile
ENST00000358273.9:c.1731G>A MANE Select	ENSP00000351015.4:p.Met577Ile
ENST00000356175.7:c.1731G>A	ENSP00000348498.3:p.Met577Ile
ENST00000358273.8:c.1731G>A	ENSP00000351015.4:p.Met577Ile
ENST00000456735.6:c.729G>A	ENSP00000389907.2:p.Met243Ile
ENST00000495910.6:c.1506G>A
ENST00000579081.5:c.1833G>A	ENSP00000462408.1:p.Met611Ile
NM_000267.3:c.1731G>A , LRG_214t1:c.1731G>A	NP_000258.1:p.Met577Ile
NM_001042492.2:c.1731G>A , LRG_214t2:c.1731G>A	NP_001035957.1:p.Met577Ile
XM_005257983.1:c.1731G>A	XP_005258040.1:p.Met577Ile
XM_005257984.1:c.1731G>A	XP_005258041.1:p.Met577Ile
XM_006721922.1:c.1761G>A	XP_006721985.1:p.Met587Ile
XM_006721923.2:c.1722G>A	XP_006721986.1:p.Met574Ile
XM_006721924.1:c.1761G>A	XP_006721987.1:p.Met587Ile
XM_006721925.1:c.1761G>A	XP_006721988.1:p.Met587Ile
XM_006721926.2:c.1761G>A	XP_006721989.1:p.Met587Ile
XM_006721927.1:c.1761G>A	XP_006721990.1:p.Met587Ile
XM_006721928.2:c.1761G>A	XP_006721991.1:p.Met587Ile
XM_011524852.1:c.1761G>A	XP_011523154.1:p.Met587Ile
XM_011524853.1:c.1722G>A	XP_011523155.1:p.Met574Ile
XM_011524854.1:c.1722G>A	XP_011523156.1:p.Met574Ile
XM_011524855.1:c.1722G>A	XP_011523157.1:p.Met574Ile
XM_011524856.1:c.1722G>A	XP_011523158.1:p.Met574Ile
XM_011524857.1:c.1761G>A	XP_011523159.1:p.Met587Ile
NM_001042492.3:c.1731G>A MANE Select	NP_001035957.1:p.Met577Ile