Canonical Allele Identifier: CA2371347802

Gene: CSTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56392982A= , CM000682.2:g.56392982A=	GRCh38
NC_000020.10:g.54968038A= , CM000682.1:g.54968038A=	GRCh37
NC_000020.9:g.54401445A=	NCBI36
NG_012133.1:g.4314T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000217109.9:c.-33+269A= MANE Select	ENSP00000217109.4:n.-33+269A=
ENST00000217109.8:c.-33+269A=	ENSP00000217109.4:n.-33+269A=
ENST00000415828.5:c.-33+444A=	ENSP00000387968.1:n.-33+444A=
ENST00000428552.1:c.-1+444A=	ENSP00000405171.1:n.-1+444A=
ENST00000452950.1:c.-33+167A=	ENSP00000409035.1:n.-33+167A=
ENST00000490539.1:c.-33+269A=	ENSP00000479273.1:n.-33+269A=
ENST00000493039.5:c.-33+167A=	ENSP00000477958.1:n.-33+167A=
ENST00000498689.5:n.168+444A=
ENST00000613138.1:n.192+269A=
NM_001033521.1:c.-33+444A=	NP_001028693.1:n.-33+444A=
NM_001033522.1:c.-33+167A=	NP_001028694.1:n.-33+167A=
NM_001324.2:c.-33+269A=	NP_001315.1:n.-33+269A=
XM_011528600.1:c.-33+243A=	XP_011526902.1:n.-33+243A=
NM_001033522.2:c.-33+167A=	NP_001028694.1:n.-33+167A=
NM_001324.3:c.-33+269A= MANE Select	NP_001315.1:n.-33+269A=
NM_001033521.2:c.-33+444A=	NP_001028693.1:n.-33+444A=