Canonical Allele Identifier: CA2371348251

Gene: CSTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56393679G= , CM000682.2:g.56393679G=	GRCh38
NC_000020.10:g.54968735G= , CM000682.1:g.54968735G=	GRCh37
NC_000020.9:g.54402142G=	NCBI36
NG_012133.1:g.3617C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001324.3:c.-33+966G= MANE Select	NP_001315.1:n.-33+966G=
ENST00000217109.9:c.-33+966G= MANE Select	ENSP00000217109.4:n.-33+966G=
NM_001033521.1:c.-33+1141G=	NP_001028693.1:n.-33+1141G=
NM_001033521.2:c.-33+1141G=	NP_001028693.1:n.-33+1141G=
NM_001033522.1:c.-33+864G=	NP_001028694.1:n.-33+864G=
NM_001033522.2:c.-33+864G=	NP_001028694.1:n.-33+864G=
NM_001324.2:c.-33+966G=	NP_001315.1:n.-33+966G=
ENST00000217109.8:c.-33+966G=	ENSP00000217109.4:n.-33+966G=
ENST00000415828.5:c.-33+1141G=	ENSP00000387968.1:n.-33+1141G=
ENST00000428552.1:c.-1+1141G=	ENSP00000405171.1:n.-1+1141G=
ENST00000452950.1:c.-33+864G=	ENSP00000409035.1:n.-33+864G=
ENST00000490539.1:c.-33+966G=	ENSP00000479273.1:n.-33+966G=
ENST00000493039.5:c.-33+864G=	ENSP00000477958.1:n.-33+864G=
ENST00000498689.5:n.168+1141G=
ENST00000613138.1:n.192+966G=
XM_011528600.1:c.-33+940G=	XP_011526902.1:n.-33+940G=