Canonical Allele Identifier: CA2371347861

Gene: CSTF1

Linked Data

• dbSNP Id: rs1987331747

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56393081C>A , CM000682.2:g.56393081C>A	GRCh38
NC_000020.10:g.54968137C>A , CM000682.1:g.54968137C>A	GRCh37
NC_000020.9:g.54401544C>A	NCBI36
NG_012133.1:g.4215G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217109.9:c.-33+368C>A MANE Select	ENSP00000217109.4:n.-33+368C>A
ENST00000217109.8:c.-33+368C>A	ENSP00000217109.4:n.-33+368C>A
ENST00000415828.5:c.-33+543C>A	ENSP00000387968.1:n.-33+543C>A
ENST00000428552.1:c.-1+543C>A	ENSP00000405171.1:n.-1+543C>A
ENST00000452950.1:c.-33+266C>A	ENSP00000409035.1:n.-33+266C>A
ENST00000490539.1:c.-33+368C>A	ENSP00000479273.1:n.-33+368C>A
ENST00000493039.5:c.-33+266C>A	ENSP00000477958.1:n.-33+266C>A
ENST00000498689.5:n.168+543C>A
ENST00000613138.1:n.192+368C>A
NM_001033521.1:c.-33+543C>A	NP_001028693.1:n.-33+543C>A
NM_001033522.1:c.-33+266C>A	NP_001028694.1:n.-33+266C>A
NM_001324.2:c.-33+368C>A	NP_001315.1:n.-33+368C>A
XM_011528600.1:c.-33+342C>A	XP_011526902.1:n.-33+342C>A
NM_001033522.2:c.-33+266C>A	NP_001028694.1:n.-33+266C>A
NM_001324.3:c.-33+368C>A MANE Select	NP_001315.1:n.-33+368C>A
NM_001033521.2:c.-33+543C>A	NP_001028693.1:n.-33+543C>A