Canonical Allele Identifier: CA499236831

Gene: NF1

Linked Data

• ClinVar Variation Id: 751419
• ClinVar RCV Id: RCV001498941
• dbSNP Id: rs1597851346
• MyVariant Identifiers: chr17:g.29670092T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31343074T>C , CM000679.2:g.31343074T>C	GRCh38
NC_000017.10:g.29670092T>C , CM000679.1:g.29670092T>C	GRCh37
NC_000017.9:g.26694218T>C	NCBI36
NG_009018.1:g.253098T>C , LRG_214:g.253098T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7110T>C	ENSP00000512431.1:p.His2370=
ENST00000684826.1:c.1692T>C	ENSP00000509994.1:p.His564=
ENST00000687027.1:c.1284T>C	ENSP00000508715.1:p.His428=
ENST00000687863.1:n.3773T>C
ENST00000689464.1:c.67T>C
ENST00000691014.1:c.7158T>C	ENSP00000510595.1:p.His2386=
ENST00000693617.1:c.1692T>C	ENSP00000510031.1:p.His564=
ENST00000358273.9:c.7128T>C MANE Select	ENSP00000351015.4:p.His2376=
ENST00000356175.7:c.7065T>C	ENSP00000348498.3:p.His2355=
ENST00000358273.8:c.7128T>C	ENSP00000351015.4:p.His2376=
ENST00000456735.6:c.6063T>C	ENSP00000389907.2:p.His2021=
ENST00000471572.6:c.511T>C
ENST00000579081.5:c.7264T>C	ENSP00000462408.1:n.7264T>C
ENST00000581790.5:c.271T>C
ENST00000582892.1:n.370T>C
ENST00000584328.1:n.542T>C
NM_000267.3:c.7065T>C , LRG_214t1:c.7065T>C	NP_000258.1:p.His2355=
NM_001042492.2:c.7128T>C , LRG_214t2:c.7128T>C	NP_001035957.1:p.His2376=
XM_005257983.1:c.7128T>C	XP_005258040.1:p.His2376=
XM_005257984.1:c.7065T>C	XP_005258041.1:p.His2355=
XM_006721922.1:c.7158T>C	XP_006721985.1:p.His2386=
XM_006721923.2:c.7119T>C	XP_006721986.1:p.His2373=
XM_006721924.1:c.7158T>C	XP_006721987.1:p.His2386=
XM_006721925.1:c.7095T>C	XP_006721988.1:p.His2365=
XM_006721926.2:c.7158T>C	XP_006721989.1:p.His2386=
XM_006721927.1:c.7158T>C	XP_006721990.1:p.His2386=
XM_011524852.1:c.7155T>C	XP_011523154.1:p.His2385=
XM_011524853.1:c.7119T>C	XP_011523155.1:p.His2373=
XM_011524854.1:c.7119T>C	XP_011523156.1:p.His2373=
XM_011524855.1:c.7119T>C	XP_011523157.1:p.His2373=
XM_011524856.1:c.7119T>C	XP_011523158.1:p.His2373=
XM_011524857.1:c.7158T>C	XP_011523159.1:p.His2386=
NM_001042492.3:c.7128T>C MANE Select	NP_001035957.1:p.His2376=