Canonical Allele Identifier: CA399000401

Gene: NF1

Linked Data

• ClinVar Variation Id: 579911
• ClinVar RCV Id: RCV000703305 ; RCV002334369
• dbSNP Id: rs1319687326
• gnomAD v2: 17-29588811-G-A
• gnomAD v4: 17-31261793-G-A
• MyVariant Identifiers: chr17:g.29588811G>A (hg19) ; chr17:g.31261793G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31261793G>A , CM000679.2:g.31261793G>A	GRCh38
NC_000017.10:g.29588811G>A , CM000679.1:g.29588811G>A	GRCh37
NC_000017.9:g.26612937G>A	NCBI36
NG_009018.1:g.171817G>A , LRG_214:g.171817G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581113.7:c.462G>A	ENSP00000492721.2:p.Leu154=
ENST00000696138.1:c.4642G>A	ENSP00000512431.1:p.Val1548Met
ENST00000696140.1:n.766G>A
ENST00000696141.1:c.651G>A
ENST00000687863.1:n.1305G>A
ENST00000691014.1:c.4690G>A	ENSP00000510595.1:p.Val1564Met
ENST00000358273.9:c.4660G>A MANE Select	ENSP00000351015.4:p.Val1554Met
ENST00000356175.7:c.4597G>A	ENSP00000348498.3:p.Val1533Met
ENST00000358273.8:c.4660G>A	ENSP00000351015.4:p.Val1554Met
ENST00000456735.6:c.3595G>A	ENSP00000389907.2:p.Val1199Met
ENST00000466819.5:c.1176G>A
ENST00000479614.1:c.1113G>A
ENST00000493220.5:n.3133G>A
ENST00000579081.5:c.4699G>A	ENSP00000462408.1:p.Val1567Met
NM_000267.3:c.4597G>A , LRG_214t1:c.4597G>A	NP_000258.1:p.Val1533Met
NM_001042492.2:c.4660G>A , LRG_214t2:c.4660G>A	NP_001035957.1:p.Val1554Met
XM_005257983.1:c.4660G>A	XP_005258040.1:p.Val1554Met
XM_005257984.1:c.4597G>A	XP_005258041.1:p.Val1533Met
XM_006721922.1:c.4690G>A	XP_006721985.1:p.Val1564Met
XM_006721923.2:c.4651G>A	XP_006721986.1:p.Val1551Met
XM_006721924.1:c.4690G>A	XP_006721987.1:p.Val1564Met
XM_006721925.1:c.4627G>A	XP_006721988.1:p.Val1543Met
XM_006721926.2:c.4690G>A	XP_006721989.1:p.Val1564Met
XM_006721927.1:c.4690G>A	XP_006721990.1:p.Val1564Met
XM_006721928.2:c.4690G>A	XP_006721991.1:p.Val1564Met
XM_011524852.1:c.4687G>A	XP_011523154.1:p.Val1563Met
XM_011524853.1:c.4651G>A	XP_011523155.1:p.Val1551Met
XM_011524854.1:c.4651G>A	XP_011523156.1:p.Val1551Met
XM_011524855.1:c.4651G>A	XP_011523157.1:p.Val1551Met
XM_011524856.1:c.4651G>A	XP_011523158.1:p.Val1551Met
XM_011524857.1:c.4690G>A	XP_011523159.1:p.Val1564Met
NM_001042492.3:c.4660G>A MANE Select	NP_001035957.1:p.Val1554Met