Canonical Allele Identifier: CA2371347858

Gene: CSTF1

Linked Data

• dbSNP Id: rs1987331487

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56393078G>A , CM000682.2:g.56393078G>A	GRCh38
NC_000020.10:g.54968134G>A , CM000682.1:g.54968134G>A	GRCh37
NC_000020.9:g.54401541G>A	NCBI36
NG_012133.1:g.4218C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217109.9:c.-33+365G>A MANE Select	ENSP00000217109.4:n.-33+365G>A
ENST00000217109.8:c.-33+365G>A	ENSP00000217109.4:n.-33+365G>A
ENST00000415828.5:c.-33+540G>A	ENSP00000387968.1:n.-33+540G>A
ENST00000428552.1:c.-1+540G>A	ENSP00000405171.1:n.-1+540G>A
ENST00000452950.1:c.-33+263G>A	ENSP00000409035.1:n.-33+263G>A
ENST00000490539.1:c.-33+365G>A	ENSP00000479273.1:n.-33+365G>A
ENST00000493039.5:c.-33+263G>A	ENSP00000477958.1:n.-33+263G>A
ENST00000498689.5:n.168+540G>A
ENST00000613138.1:n.192+365G>A
NM_001033521.1:c.-33+540G>A	NP_001028693.1:n.-33+540G>A
NM_001033522.1:c.-33+263G>A	NP_001028694.1:n.-33+263G>A
NM_001324.2:c.-33+365G>A	NP_001315.1:n.-33+365G>A
XM_011528600.1:c.-33+339G>A	XP_011526902.1:n.-33+339G>A
NM_001033522.2:c.-33+263G>A	NP_001028694.1:n.-33+263G>A
NM_001324.3:c.-33+365G>A MANE Select	NP_001315.1:n.-33+365G>A
NM_001033521.2:c.-33+540G>A	NP_001028693.1:n.-33+540G>A