Canonical Allele Identifier: CA2371347743

Gene: CSTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56392885G= , CM000682.2:g.56392885G=	GRCh38
NC_000020.10:g.54967941G= , CM000682.1:g.54967941G=	GRCh37
NC_000020.9:g.54401348G=	NCBI36
NG_012133.1:g.4411C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000217109.9:c.-33+172G= MANE Select	ENSP00000217109.4:n.-33+172G=
ENST00000217109.8:c.-33+172G=	ENSP00000217109.4:n.-33+172G=
ENST00000415828.5:c.-33+347G=	ENSP00000387968.1:n.-33+347G=
ENST00000428552.1:c.-1+347G=	ENSP00000405171.1:n.-1+347G=
ENST00000452950.1:c.-33+70G=	ENSP00000409035.1:n.-33+70G=
ENST00000490539.1:c.-33+172G=	ENSP00000479273.1:n.-33+172G=
ENST00000493039.5:c.-33+70G=	ENSP00000477958.1:n.-33+70G=
ENST00000498689.5:n.168+347G=
ENST00000613138.1:n.192+172G=
NM_001033521.1:c.-33+347G=	NP_001028693.1:n.-33+347G=
NM_001033522.1:c.-33+70G=	NP_001028694.1:n.-33+70G=
NM_001324.2:c.-33+172G=	NP_001315.1:n.-33+172G=
XM_011528600.1:c.-33+146G=	XP_011526902.1:n.-33+146G=
NM_001033522.2:c.-33+70G=	NP_001028694.1:n.-33+70G=
NM_001324.3:c.-33+172G= MANE Select	NP_001315.1:n.-33+172G=
NM_001033521.2:c.-33+347G=	NP_001028693.1:n.-33+347G=