Canonical Allele Identifier: CA2371347811

Gene: CSTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56392998G= , CM000682.2:g.56392998G=	GRCh38
NC_000020.10:g.54968054G= , CM000682.1:g.54968054G=	GRCh37
NC_000020.9:g.54401461G=	NCBI36
NG_012133.1:g.4298C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000217109.9:c.-33+285G= MANE Select	ENSP00000217109.4:n.-33+285G=
ENST00000217109.8:c.-33+285G=	ENSP00000217109.4:n.-33+285G=
ENST00000415828.5:c.-33+460G=	ENSP00000387968.1:n.-33+460G=
ENST00000428552.1:c.-1+460G=	ENSP00000405171.1:n.-1+460G=
ENST00000452950.1:c.-33+183G=	ENSP00000409035.1:n.-33+183G=
ENST00000490539.1:c.-33+285G=	ENSP00000479273.1:n.-33+285G=
ENST00000493039.5:c.-33+183G=	ENSP00000477958.1:n.-33+183G=
ENST00000498689.5:n.168+460G=
ENST00000613138.1:n.192+285G=
NM_001033521.1:c.-33+460G=	NP_001028693.1:n.-33+460G=
NM_001033522.1:c.-33+183G=	NP_001028694.1:n.-33+183G=
NM_001324.2:c.-33+285G=	NP_001315.1:n.-33+285G=
XM_011528600.1:c.-33+259G=	XP_011526902.1:n.-33+259G=
NM_001033522.2:c.-33+183G=	NP_001028694.1:n.-33+183G=
NM_001324.3:c.-33+285G= MANE Select	NP_001315.1:n.-33+285G=
NM_001033521.2:c.-33+460G=	NP_001028693.1:n.-33+460G=