Canonical Allele Identifier: CA377335443

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759758G>T (hg19) ; chr10:g.78000000G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000000G>T , CM000672.2:g.78000000G>T	GRCh38
NC_000010.10:g.79759758G>T , CM000672.1:g.79759758G>T	GRCh37
NC_000010.9:g.79429764G>T	NCBI36
NG_029648.1:g.34541C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1657C>A
ENST00000698728.1:n.2176C>A
ENST00000698729.1:n.3722C>A
ENST00000698730.1:n.3722C>A
ENST00000698731.1:c.2456C>A	ENSP00000513898.1:p.Ala819Asp
ENST00000698732.1:c.*1458C>A	ENSP00000513899.1:n.*1458C>A
ENST00000698733.1:c.*1784C>A	ENSP00000513900.1:n.*1784C>A
ENST00000698734.1:c.2597C>A	ENSP00000513901.1:p.Ala866Asp
ENST00000698735.1:n.2712C>A
ENST00000698736.1:n.2712C>A
ENST00000698737.1:n.2712C>A
ENST00000698738.1:n.2712C>A
ENST00000698739.1:n.2712C>A
ENST00000372371.8:c.2597C>A MANE Select	ENSP00000361446.3:p.Ala866Asp
ENST00000372371.7:c.2597C>A	ENSP00000361446.3:p.Ala866Asp
ENST00000472014.5:n.469+4716C>A
NM_007055.3:c.2597C>A	NP_008986.2:p.Ala866Asp
NM_007055.4:c.2597C>A MANE Select	NP_008986.2:p.Ala866Asp