Canonical Allele Identifier: CA316165382

Gene: CSTF1

Linked Data

• dbSNP Id: rs1003431733
• MyVariant Identifiers: chr20:g.54968141G>A (hg19) ; chr20:g.56393085G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56393085G>A , CM000682.2:g.56393085G>A	GRCh38
NC_000020.10:g.54968141G>A , CM000682.1:g.54968141G>A	GRCh37
NC_000020.9:g.54401548G>A	NCBI36
NG_012133.1:g.4211C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000217109.9:c.-33+372G>A MANE Select	ENSP00000217109.4:n.-33+372G>A
ENST00000217109.8:c.-33+372G>A	ENSP00000217109.4:n.-33+372G>A
ENST00000415828.5:c.-33+547G>A	ENSP00000387968.1:n.-33+547G>A
ENST00000428552.1:c.-1+547G>A	ENSP00000405171.1:n.-1+547G>A
ENST00000452950.1:c.-33+270G>A	ENSP00000409035.1:n.-33+270G>A
ENST00000490539.1:c.-33+372G>A	ENSP00000479273.1:n.-33+372G>A
ENST00000493039.5:c.-33+270G>A	ENSP00000477958.1:n.-33+270G>A
ENST00000498689.5:n.168+547G>A
ENST00000613138.1:n.192+372G>A
NM_001033521.1:c.-33+547G>A	NP_001028693.1:n.-33+547G>A
NM_001033522.1:c.-33+270G>A	NP_001028694.1:n.-33+270G>A
NM_001324.2:c.-33+372G>A	NP_001315.1:n.-33+372G>A
XM_011528600.1:c.-33+346G>A	XP_011526902.1:n.-33+346G>A
NM_001033522.2:c.-33+270G>A	NP_001028694.1:n.-33+270G>A
NM_001324.3:c.-33+372G>A MANE Select	NP_001315.1:n.-33+372G>A
NM_001033521.2:c.-33+547G>A	NP_001028693.1:n.-33+547G>A