Canonical Allele Identifier: CA2371349440

Gene: CSTF1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56396330G>A , CM000682.2:g.56396330G>A	GRCh38
NC_000020.10:g.54971386G>A , CM000682.1:g.54971386G>A	GRCh37
NC_000020.9:g.54404793G>A	NCBI36
NG_012133.1:g.966C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217109.9:c.169+609G>A MANE Select	ENSP00000217109.4:n.169+609G>A
ENST00000217109.8:c.169+609G>A	ENSP00000217109.4:n.169+609G>A
ENST00000415828.5:c.169+609G>A	ENSP00000387968.1:n.169+609G>A
ENST00000428552.1:c.169+609G>A	ENSP00000405171.1:n.169+609G>A
ENST00000452950.1:c.169+609G>A	ENSP00000409035.1:n.169+609G>A
ENST00000490539.1:c.*27+571G>A	ENSP00000479273.1:n.*27+571G>A
ENST00000493039.5:c.*27+571G>A	ENSP00000477958.1:n.*27+571G>A
ENST00000613138.1:n.394-588G>A
NM_001033521.1:c.169+609G>A	NP_001028693.1:n.169+609G>A
NM_001033522.1:c.169+609G>A	NP_001028694.1:n.169+609G>A
NM_001324.2:c.169+609G>A	NP_001315.1:n.169+609G>A
XM_011528600.1:c.169+609G>A	XP_011526902.1:n.169+609G>A
NM_001033522.2:c.169+609G>A	NP_001028694.1:n.169+609G>A
NM_001324.3:c.169+609G>A MANE Select	NP_001315.1:n.169+609G>A
NM_001033521.2:c.169+609G>A	NP_001028693.1:n.169+609G>A