Canonical Allele Identifier: CA377335625

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759827G>T (hg19) ; chr10:g.78000069G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000069G>T , CM000672.2:g.78000069G>T	GRCh38
NC_000010.10:g.79759827G>T , CM000672.1:g.79759827G>T	GRCh37
NC_000010.9:g.79429833G>T	NCBI36
NG_029648.1:g.34472C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1588C>A
ENST00000698728.1:n.2107C>A
ENST00000698729.1:n.3653C>A
ENST00000698730.1:n.3653C>A
ENST00000698731.1:c.2387C>A	ENSP00000513898.1:p.Thr796Lys
ENST00000698732.1:c.*1389C>A	ENSP00000513899.1:n.*1389C>A
ENST00000698733.1:c.*1715C>A	ENSP00000513900.1:n.*1715C>A
ENST00000698734.1:c.2528C>A	ENSP00000513901.1:p.Thr843Lys
ENST00000698735.1:n.2643C>A
ENST00000698736.1:n.2643C>A
ENST00000698737.1:n.2643C>A
ENST00000698738.1:n.2643C>A
ENST00000698739.1:n.2643C>A
ENST00000372371.8:c.2528C>A MANE Select	ENSP00000361446.3:p.Thr843Lys
ENST00000372371.7:c.2528C>A	ENSP00000361446.3:p.Thr843Lys
ENST00000472014.5:n.469+4647C>A
NM_007055.3:c.2528C>A	NP_008986.2:p.Thr843Lys
NM_007055.4:c.2528C>A MANE Select	NP_008986.2:p.Thr843Lys