Canonical Allele Identifier: CA377340920

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769632G>T (hg19) ; chr10:g.78009874G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009874G>T , CM000672.2:g.78009874G>T	GRCh38
NC_000010.10:g.79769632G>T , CM000672.1:g.79769632G>T	GRCh37
NC_000010.9:g.79439638G>T	NCBI36
NG_029648.1:g.24667C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698728.1:n.1339C>A
ENST00000698729.1:n.2885C>A
ENST00000698730.1:n.2885C>A
ENST00000698731.1:c.1619C>A	ENSP00000513898.1:p.Thr540Lys
ENST00000698732.1:c.*621C>A	ENSP00000513899.1:n.*621C>A
ENST00000698733.1:c.*947C>A	ENSP00000513900.1:n.*947C>A
ENST00000698734.1:c.1760C>A	ENSP00000513901.1:p.Thr587Lys
ENST00000698735.1:n.1875C>A
ENST00000698736.1:n.1875C>A
ENST00000698737.1:n.1875C>A
ENST00000698738.1:n.1875C>A
ENST00000698739.1:n.1875C>A
ENST00000372371.8:c.1760C>A MANE Select	ENSP00000361446.3:p.Thr587Lys
ENST00000372371.7:c.1760C>A	ENSP00000361446.3:p.Thr587Lys
ENST00000473588.2:c.562C>A
NM_007055.3:c.1760C>A	NP_008986.2:p.Thr587Lys
NM_007055.4:c.1760C>A MANE Select	NP_008986.2:p.Thr587Lys