Canonical Allele Identifier: CA2653411106

Gene: CSTF1

Linked Data

• gnomAD v4: 20-56392904-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56392904A>T , CM000682.2:g.56392904A>T	GRCh38
NC_000020.10:g.54967960A>T , CM000682.1:g.54967960A>T	GRCh37
NC_000020.9:g.54401367A>T	NCBI36
NG_012133.1:g.4392T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217109.9:c.-33+191A>T MANE Select	ENSP00000217109.4:n.-33+191A>T
ENST00000217109.8:c.-33+191A>T	ENSP00000217109.4:n.-33+191A>T
ENST00000415828.5:c.-33+366A>T	ENSP00000387968.1:n.-33+366A>T
ENST00000428552.1:c.-1+366A>T	ENSP00000405171.1:n.-1+366A>T
ENST00000452950.1:c.-33+89A>T	ENSP00000409035.1:n.-33+89A>T
ENST00000490539.1:c.-33+191A>T	ENSP00000479273.1:n.-33+191A>T
ENST00000493039.5:c.-33+89A>T	ENSP00000477958.1:n.-33+89A>T
ENST00000498689.5:n.168+366A>T
ENST00000613138.1:n.192+191A>T
NM_001033521.1:c.-33+366A>T	NP_001028693.1:n.-33+366A>T
NM_001033522.1:c.-33+89A>T	NP_001028694.1:n.-33+89A>T
NM_001324.2:c.-33+191A>T	NP_001315.1:n.-33+191A>T
XM_011528600.1:c.-33+165A>T	XP_011526902.1:n.-33+165A>T
NM_001033522.2:c.-33+89A>T	NP_001028694.1:n.-33+89A>T
NM_001324.3:c.-33+191A>T MANE Select	NP_001315.1:n.-33+191A>T
NM_001033521.2:c.-33+366A>T	NP_001028693.1:n.-33+366A>T