Canonical Allele Identifier: CA377335651

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759833C>T (hg19) ; chr10:g.78000075C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000075C>T , CM000672.2:g.78000075C>T	GRCh38
NC_000010.10:g.79759833C>T , CM000672.1:g.79759833C>T	GRCh37
NC_000010.9:g.79429839C>T	NCBI36
NG_029648.1:g.34466G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1582G>A
ENST00000698728.1:n.2101G>A
ENST00000698729.1:n.3647G>A
ENST00000698730.1:n.3647G>A
ENST00000698731.1:c.2381G>A	ENSP00000513898.1:p.Gly794Asp
ENST00000698732.1:c.*1383G>A	ENSP00000513899.1:n.*1383G>A
ENST00000698733.1:c.*1709G>A	ENSP00000513900.1:n.*1709G>A
ENST00000698734.1:c.2522G>A	ENSP00000513901.1:p.Gly841Asp
ENST00000698735.1:n.2637G>A
ENST00000698736.1:n.2637G>A
ENST00000698737.1:n.2637G>A
ENST00000698738.1:n.2637G>A
ENST00000698739.1:n.2637G>A
ENST00000372371.8:c.2522G>A MANE Select	ENSP00000361446.3:p.Gly841Asp
ENST00000372371.7:c.2522G>A	ENSP00000361446.3:p.Gly841Asp
ENST00000472014.5:n.469+4641G>A
NM_007055.3:c.2522G>A	NP_008986.2:p.Gly841Asp
NM_007055.4:c.2522G>A MANE Select	NP_008986.2:p.Gly841Asp