Canonical Allele Identifier: CA2371347774

Gene: CSTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56392929T= , CM000682.2:g.56392929T=	GRCh38
NC_000020.10:g.54967985T= , CM000682.1:g.54967985T=	GRCh37
NC_000020.9:g.54401392T=	NCBI36
NG_012133.1:g.4367A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000217109.9:c.-33+216T= MANE Select	ENSP00000217109.4:n.-33+216T=
ENST00000217109.8:c.-33+216T=	ENSP00000217109.4:n.-33+216T=
ENST00000415828.5:c.-33+391T=	ENSP00000387968.1:n.-33+391T=
ENST00000428552.1:c.-1+391T=	ENSP00000405171.1:n.-1+391T=
ENST00000452950.1:c.-33+114T=	ENSP00000409035.1:n.-33+114T=
ENST00000490539.1:c.-33+216T=	ENSP00000479273.1:n.-33+216T=
ENST00000493039.5:c.-33+114T=	ENSP00000477958.1:n.-33+114T=
ENST00000498689.5:n.168+391T=
ENST00000613138.1:n.192+216T=
NM_001033521.1:c.-33+391T=	NP_001028693.1:n.-33+391T=
NM_001033522.1:c.-33+114T=	NP_001028694.1:n.-33+114T=
NM_001324.2:c.-33+216T=	NP_001315.1:n.-33+216T=
XM_011528600.1:c.-33+190T=	XP_011526902.1:n.-33+190T=
NM_001033522.2:c.-33+114T=	NP_001028694.1:n.-33+114T=
NM_001324.3:c.-33+216T= MANE Select	NP_001315.1:n.-33+216T=
NM_001033521.2:c.-33+391T=	NP_001028693.1:n.-33+391T=