Canonical Allele Identifier: CA2371347839

Gene: CSTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56393040T= , CM000682.2:g.56393040T=	GRCh38
NC_000020.10:g.54968096T= , CM000682.1:g.54968096T=	GRCh37
NC_000020.9:g.54401503T=	NCBI36
NG_012133.1:g.4256A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000217109.9:c.-33+327T= MANE Select	ENSP00000217109.4:n.-33+327T=
ENST00000217109.8:c.-33+327T=	ENSP00000217109.4:n.-33+327T=
ENST00000415828.5:c.-33+502T=	ENSP00000387968.1:n.-33+502T=
ENST00000428552.1:c.-1+502T=	ENSP00000405171.1:n.-1+502T=
ENST00000452950.1:c.-33+225T=	ENSP00000409035.1:n.-33+225T=
ENST00000490539.1:c.-33+327T=	ENSP00000479273.1:n.-33+327T=
ENST00000493039.5:c.-33+225T=	ENSP00000477958.1:n.-33+225T=
ENST00000498689.5:n.168+502T=
ENST00000613138.1:n.192+327T=
NM_001033521.1:c.-33+502T=	NP_001028693.1:n.-33+502T=
NM_001033522.1:c.-33+225T=	NP_001028694.1:n.-33+225T=
NM_001324.2:c.-33+327T=	NP_001315.1:n.-33+327T=
XM_011528600.1:c.-33+301T=	XP_011526902.1:n.-33+301T=
NM_001033522.2:c.-33+225T=	NP_001028694.1:n.-33+225T=
NM_001324.3:c.-33+327T= MANE Select	NP_001315.1:n.-33+327T=
NM_001033521.2:c.-33+502T=	NP_001028693.1:n.-33+502T=