Canonical Allele Identifier: CA745792987

Gene: CSTF1

Linked Data

• dbSNP Id: rs1382495507
• gnomAD v3: 20-56393020-T-A
• gnomAD v4: 20-56393020-T-A
• MyVariant Identifiers: chr20:g.54968076T>A (hg19) ; chr20:g.56393020T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56393020T>A , CM000682.2:g.56393020T>A	GRCh38
NC_000020.10:g.54968076T>A , CM000682.1:g.54968076T>A	GRCh37
NC_000020.9:g.54401483T>A	NCBI36
NG_012133.1:g.4276A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000217109.9:c.-33+307T>A MANE Select	ENSP00000217109.4:n.-33+307T>A
ENST00000217109.8:c.-33+307T>A	ENSP00000217109.4:n.-33+307T>A
ENST00000415828.5:c.-33+482T>A	ENSP00000387968.1:n.-33+482T>A
ENST00000428552.1:c.-1+482T>A	ENSP00000405171.1:n.-1+482T>A
ENST00000452950.1:c.-33+205T>A	ENSP00000409035.1:n.-33+205T>A
ENST00000490539.1:c.-33+307T>A	ENSP00000479273.1:n.-33+307T>A
ENST00000493039.5:c.-33+205T>A	ENSP00000477958.1:n.-33+205T>A
ENST00000498689.5:n.168+482T>A
ENST00000613138.1:n.192+307T>A
NM_001033521.1:c.-33+482T>A	NP_001028693.1:n.-33+482T>A
NM_001033522.1:c.-33+205T>A	NP_001028694.1:n.-33+205T>A
NM_001324.2:c.-33+307T>A	NP_001315.1:n.-33+307T>A
XM_011528600.1:c.-33+281T>A	XP_011526902.1:n.-33+281T>A
NM_001033522.2:c.-33+205T>A	NP_001028694.1:n.-33+205T>A
NM_001324.3:c.-33+307T>A MANE Select	NP_001315.1:n.-33+307T>A
NM_001033521.2:c.-33+482T>A	NP_001028693.1:n.-33+482T>A