Canonical Allele Identifier: CA399203481

Gene: NF1

Linked Data

• dbSNP Id: rs2151583339
• MyVariant Identifiers: chr17:g.29684346A>T (hg19) ; chr17:g.31357328A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31357328A>T , CM000679.2:g.31357328A>T	GRCh38
NC_000017.10:g.29684346A>T , CM000679.1:g.29684346A>T	GRCh37
NC_000017.9:g.26708472A>T	NCBI36
NG_009018.1:g.267352A>T , LRG_214:g.267352A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7911A>T	ENSP00000512431.1:p.Leu2637Phe
ENST00000684826.1:c.2493A>T	ENSP00000509994.1:p.Leu831Phe
ENST00000687027.1:c.2085A>T	ENSP00000508715.1:p.Leu695Phe
ENST00000687863.1:n.4574A>T
ENST00000689464.1:c.979A>T
ENST00000691014.1:c.7959A>T	ENSP00000510595.1:p.Leu2653Phe
ENST00000693617.1:c.2493A>T	ENSP00000510031.1:p.Leu831Phe
ENST00000358273.9:c.7929A>T MANE Select	ENSP00000351015.4:p.Leu2643Phe
ENST00000356175.7:c.7866A>T	ENSP00000348498.3:p.Leu2622Phe
ENST00000358273.8:c.7929A>T	ENSP00000351015.4:p.Leu2643Phe
ENST00000456735.6:c.6864A>T	ENSP00000389907.2:p.Leu2288Phe
ENST00000471572.6:c.1312A>T
ENST00000577967.1:n.1525A>T
ENST00000579081.5:c.8065A>T	ENSP00000462408.1:n.8065A>T
ENST00000581790.5:c.914A>T
NM_000267.3:c.7866A>T , LRG_214t1:c.7866A>T	NP_000258.1:p.Leu2622Phe
NM_001042492.2:c.7929A>T , LRG_214t2:c.7929A>T	NP_001035957.1:p.Leu2643Phe
XM_005257983.1:c.7929A>T	XP_005258040.1:p.Leu2643Phe
XM_005257984.1:c.7866A>T	XP_005258041.1:p.Leu2622Phe
XM_006721922.1:c.7959A>T	XP_006721985.1:p.Leu2653Phe
XM_006721923.2:c.7920A>T	XP_006721986.1:p.Leu2640Phe
XM_006721924.1:c.7959A>T	XP_006721987.1:p.Leu2653Phe
XM_006721925.1:c.7896A>T	XP_006721988.1:p.Leu2632Phe
XM_006721926.2:c.7959A>T	XP_006721989.1:p.Leu2653Phe
XM_006721927.1:c.7959A>T	XP_006721990.1:p.Leu2653Phe
XM_011524852.1:c.7956A>T	XP_011523154.1:p.Leu2652Phe
XM_011524853.1:c.7920A>T	XP_011523155.1:p.Leu2640Phe
XM_011524854.1:c.7920A>T	XP_011523156.1:p.Leu2640Phe
XM_011524855.1:c.7920A>T	XP_011523157.1:p.Leu2640Phe
XM_011524856.1:c.7920A>T	XP_011523158.1:p.Leu2640Phe
XM_011524857.1:c.7836A>T	XP_011523159.1:p.Leu2612Phe
NM_001042492.3:c.7929A>T MANE Select	NP_001035957.1:p.Leu2643Phe