Canonical Allele Identifier: CA745792901

Gene: CSTF1

Linked Data

• dbSNP Id: rs1274163896
• gnomAD v4: 20-56392902-C-T
• MyVariant Identifiers: chr20:g.54967958C>T (hg19) ; chr20:g.56392902C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56392902C>T , CM000682.2:g.56392902C>T	GRCh38
NC_000020.10:g.54967958C>T , CM000682.1:g.54967958C>T	GRCh37
NC_000020.9:g.54401365C>T	NCBI36
NG_012133.1:g.4394G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000217109.9:c.-33+189C>T MANE Select	ENSP00000217109.4:n.-33+189C>T
ENST00000217109.8:c.-33+189C>T	ENSP00000217109.4:n.-33+189C>T
ENST00000415828.5:c.-33+364C>T	ENSP00000387968.1:n.-33+364C>T
ENST00000428552.1:c.-1+364C>T	ENSP00000405171.1:n.-1+364C>T
ENST00000452950.1:c.-33+87C>T	ENSP00000409035.1:n.-33+87C>T
ENST00000490539.1:c.-33+189C>T	ENSP00000479273.1:n.-33+189C>T
ENST00000493039.5:c.-33+87C>T	ENSP00000477958.1:n.-33+87C>T
ENST00000498689.5:n.168+364C>T
ENST00000613138.1:n.192+189C>T
NM_001033521.1:c.-33+364C>T	NP_001028693.1:n.-33+364C>T
NM_001033522.1:c.-33+87C>T	NP_001028694.1:n.-33+87C>T
NM_001324.2:c.-33+189C>T	NP_001315.1:n.-33+189C>T
XM_011528600.1:c.-33+163C>T	XP_011526902.1:n.-33+163C>T
NM_001033522.2:c.-33+87C>T	NP_001028694.1:n.-33+87C>T
NM_001324.3:c.-33+189C>T MANE Select	NP_001315.1:n.-33+189C>T
NM_001033521.2:c.-33+364C>T	NP_001028693.1:n.-33+364C>T