Canonical Allele Identifier: CA2371347829

Gene: CSTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56393025T= , CM000682.2:g.56393025T=	GRCh38
NC_000020.10:g.54968081T= , CM000682.1:g.54968081T=	GRCh37
NC_000020.9:g.54401488T=	NCBI36
NG_012133.1:g.4271A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000217109.9:c.-33+312T= MANE Select	ENSP00000217109.4:n.-33+312T=
ENST00000217109.8:c.-33+312T=	ENSP00000217109.4:n.-33+312T=
ENST00000415828.5:c.-33+487T=	ENSP00000387968.1:n.-33+487T=
ENST00000428552.1:c.-1+487T=	ENSP00000405171.1:n.-1+487T=
ENST00000452950.1:c.-33+210T=	ENSP00000409035.1:n.-33+210T=
ENST00000490539.1:c.-33+312T=	ENSP00000479273.1:n.-33+312T=
ENST00000493039.5:c.-33+210T=	ENSP00000477958.1:n.-33+210T=
ENST00000498689.5:n.168+487T=
ENST00000613138.1:n.192+312T=
NM_001033521.1:c.-33+487T=	NP_001028693.1:n.-33+487T=
NM_001033522.1:c.-33+210T=	NP_001028694.1:n.-33+210T=
NM_001324.2:c.-33+312T=	NP_001315.1:n.-33+312T=
XM_011528600.1:c.-33+286T=	XP_011526902.1:n.-33+286T=
NM_001033522.2:c.-33+210T=	NP_001028694.1:n.-33+210T=
NM_001324.3:c.-33+312T= MANE Select	NP_001315.1:n.-33+312T=
NM_001033521.2:c.-33+487T=	NP_001028693.1:n.-33+487T=