Canonical Allele Identifier: CA499239071

Gene: NF1

Linked Data

• ClinVar Variation Id: 1650646
• ClinVar RCV Id: RCV002149122
• dbSNP Id: rs2151572549
• gnomAD v4: 17-31349145-T-C
• MyVariant Identifiers: chr17:g.29676163T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31349145T>C , CM000679.2:g.31349145T>C	GRCh38
NC_000017.10:g.29676163T>C , CM000679.1:g.29676163T>C	GRCh37
NC_000017.9:g.26700289T>C	NCBI36
NG_009018.1:g.259169T>C , LRG_214:g.259169T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7197T>C	ENSP00000512431.1:p.Ile2399=
ENST00000684826.1:c.1779T>C	ENSP00000509994.1:p.Ile593=
ENST00000687027.1:c.1371T>C	ENSP00000508715.1:p.Ile457=
ENST00000687863.1:n.3860T>C
ENST00000689464.1:c.265T>C
ENST00000691014.1:c.7245T>C	ENSP00000510595.1:p.Ile2415=
ENST00000693617.1:c.1779T>C	ENSP00000510031.1:p.Ile593=
ENST00000358273.9:c.7215T>C MANE Select	ENSP00000351015.4:p.Ile2405=
ENST00000356175.7:c.7152T>C	ENSP00000348498.3:p.Ile2384=
ENST00000358273.8:c.7215T>C	ENSP00000351015.4:p.Ile2405=
ENST00000456735.6:c.6150T>C	ENSP00000389907.2:p.Ile2050=
ENST00000471572.6:c.598T>C
ENST00000579081.5:c.7351T>C	ENSP00000462408.1:n.7351T>C
ENST00000581790.5:c.358T>C
ENST00000582892.1:n.457T>C
NM_000267.3:c.7152T>C , LRG_214t1:c.7152T>C	NP_000258.1:p.Ile2384=
NM_001042492.2:c.7215T>C , LRG_214t2:c.7215T>C	NP_001035957.1:p.Ile2405=
XM_005257983.1:c.7215T>C	XP_005258040.1:p.Ile2405=
XM_005257984.1:c.7152T>C	XP_005258041.1:p.Ile2384=
XM_006721922.1:c.7245T>C	XP_006721985.1:p.Ile2415=
XM_006721923.2:c.7206T>C	XP_006721986.1:p.Ile2402=
XM_006721924.1:c.7245T>C	XP_006721987.1:p.Ile2415=
XM_006721925.1:c.7182T>C	XP_006721988.1:p.Ile2394=
XM_006721926.2:c.7245T>C	XP_006721989.1:p.Ile2415=
XM_006721927.1:c.7245T>C	XP_006721990.1:p.Ile2415=
XM_011524852.1:c.7242T>C	XP_011523154.1:p.Ile2414=
XM_011524853.1:c.7206T>C	XP_011523155.1:p.Ile2402=
XM_011524854.1:c.7206T>C	XP_011523156.1:p.Ile2402=
XM_011524855.1:c.7206T>C	XP_011523157.1:p.Ile2402=
XM_011524856.1:c.7206T>C	XP_011523158.1:p.Ile2402=
XM_011524857.1:c.7245T>C	XP_011523159.1:p.Ile2415=
NM_001042492.3:c.7215T>C MANE Select	NP_001035957.1:p.Ile2405=