Canonical Allele Identifier: CA1950895188

Gene: EIF3F

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.7993230G= , CM000673.2:g.7993230G=	GRCh38
NC_000011.9:g.8014777G= , CM000673.1:g.8014777G=	GRCh37
NC_000011.8:g.7971353G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003754.3:c.653+206G= MANE Select	NP_003745.1:n.653+206G=
ENST00000651655.1:c.653+206G= MANE Select	ENSP00000499218.1:n.653+206G=
NM_003754.2:c.653+206G=	NP_003745.1:n.653+206G=
ENST00000309828.4:c.653+206G=	ENSP00000310040.4:n.653+206G=
ENST00000528653.2:n.658+206G=
ENST00000528763.2:n.408+206G=
ENST00000530219.1:n.830+206G=
ENST00000530219.2:n.453+206G=
ENST00000531329.5:c.*207+206G=	ENSP00000432489.1:n.*207+206G=
ENST00000531329.6:c.*97+206G=	ENSP00000432489.2:n.*97+206G=
ENST00000531572.2:c.653+206G=	ENSP00000434286.2:n.653+206G=
ENST00000532882.2:n.2022+206G=
ENST00000533626.5:c.653+206G=	ENSP00000431800.1:n.653+206G=
ENST00000640290.2:c.*254+206G=	ENSP00000491198.2:n.*254+206G=
ENST00000677121.1:c.653+206G=	ENSP00000503130.1:n.653+206G=
ENST00000677179.1:n.4945+206G=
ENST00000677795.1:n.2224+206G=
ENST00000677866.1:n.503G=
ENST00000678132.1:c.*254+206G=	ENSP00000504073.1:n.*254+206G=
ENST00000678993.1:c.*207+206G=	ENSP00000504201.1:n.*207+206G=