Canonical Allele Identifier: CA399206084

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31374123T>C , CM000679.2:g.31374123T>C	GRCh38
NC_000017.10:g.29701141T>C , CM000679.1:g.29701141T>C	GRCh37
NC_000017.9:g.26725267T>C	NCBI36
NG_009018.1:g.284147T>C , LRG_214:g.284147T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001042492.3:c.8488T>C MANE Select	NP_001035957.1:p.Phe2830Leu
ENST00000358273.9:c.8488T>C MANE Select	ENSP00000351015.4:p.Phe2830Leu
NM_000267.3:c.8425T>C , LRG_214t1:c.8425T>C	NP_000258.1:p.Phe2809Leu
NM_001042492.2:c.8488T>C , LRG_214t2:c.8488T>C	NP_001035957.1:p.Phe2830Leu
ENST00000356175.7:c.8425T>C	ENSP00000348498.3:p.Phe2809Leu
ENST00000358273.8:c.8488T>C	ENSP00000351015.4:p.Phe2830Leu
ENST00000456735.6:c.7477T>C	ENSP00000389907.2:p.Phe2493Leu
ENST00000471572.6:c.1871T>C
ENST00000579081.5:c.8624T>C	ENSP00000462408.1:n.8624T>C
ENST00000684826.1:c.3106T>C	ENSP00000509994.1:p.Phe1036Leu
ENST00000687027.1:c.2644T>C	ENSP00000508715.1:p.Phe882Leu
ENST00000689464.1:c.1592T>C
ENST00000691014.1:c.8518T>C	ENSP00000510595.1:p.Phe2840Leu
ENST00000693617.1:c.3052T>C	ENSP00000510031.1:p.Phe1018Leu
ENST00000696138.1:c.*123T>C	ENSP00000512431.1:n.*123T>C
XM_005257983.1:c.8542T>C	XP_005258040.1:p.Phe2848Leu
XM_005257984.1:c.8479T>C	XP_005258041.1:p.Phe2827Leu
XM_006721922.1:c.8572T>C	XP_006721985.1:p.Phe2858Leu
XM_006721923.2:c.8533T>C	XP_006721986.1:p.Phe2845Leu
XM_006721924.1:c.8518T>C	XP_006721987.1:p.Phe2840Leu
XM_006721925.1:c.8509T>C	XP_006721988.1:p.Phe2837Leu
XM_011524852.1:c.8569T>C	XP_011523154.1:p.Phe2857Leu
XM_011524853.1:c.8533T>C	XP_011523155.1:p.Phe2845Leu
XM_011524854.1:c.8533T>C	XP_011523156.1:p.Phe2845Leu
XM_011524855.1:c.8533T>C	XP_011523157.1:p.Phe2845Leu
XM_011524856.1:c.8533T>C	XP_011523158.1:p.Phe2845Leu
XM_011524857.1:c.8449T>C	XP_011523159.1:p.Phe2817Leu