Canonical Allele Identifier: CA377340919

Gene: POLR3A

Linked Data

• dbSNP Id: rs1437084847
• MyVariant Identifiers: chr10:g.79769632G>A (hg19) ; chr10:g.78009874G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698728.1:n.1339C>T
ENST00000698729.1:n.2885C>T
ENST00000698730.1:n.2885C>T
ENST00000698731.1:c.1619C>T	ENSP00000513898.1:p.Thr540Ile
ENST00000698732.1:c.*621C>T	ENSP00000513899.1:n.*621C>T
ENST00000698733.1:c.*947C>T	ENSP00000513900.1:n.*947C>T
ENST00000698734.1:c.1760C>T	ENSP00000513901.1:p.Thr587Ile
ENST00000698735.1:n.1875C>T
ENST00000698736.1:n.1875C>T
ENST00000698737.1:n.1875C>T
ENST00000698738.1:n.1875C>T
ENST00000698739.1:n.1875C>T
ENST00000372371.8:c.1760C>T MANE Select	ENSP00000361446.3:p.Thr587Ile
ENST00000372371.7:c.1760C>T	ENSP00000361446.3:p.Thr587Ile
ENST00000473588.2:c.562C>T
NM_007055.3:c.1760C>T	NP_008986.2:p.Thr587Ile
NM_007055.4:c.1760C>T MANE Select	NP_008986.2:p.Thr587Ile