Canonical Allele Identifier: CA377335695

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759843A>C (hg19) ; chr10:g.78000085A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000085A>C , CM000672.2:g.78000085A>C	GRCh38
NC_000010.10:g.79759843A>C , CM000672.1:g.79759843A>C	GRCh37
NC_000010.9:g.79429849A>C	NCBI36
NG_029648.1:g.34456T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1572T>G
ENST00000698728.1:n.2091T>G
ENST00000698729.1:n.3637T>G
ENST00000698730.1:n.3637T>G
ENST00000698731.1:c.2371T>G	ENSP00000513898.1:p.Phe791Val
ENST00000698732.1:c.*1373T>G	ENSP00000513899.1:n.*1373T>G
ENST00000698733.1:c.*1699T>G	ENSP00000513900.1:n.*1699T>G
ENST00000698734.1:c.2512T>G	ENSP00000513901.1:p.Phe838Val
ENST00000698735.1:n.2627T>G
ENST00000698736.1:n.2627T>G
ENST00000698737.1:n.2627T>G
ENST00000698738.1:n.2627T>G
ENST00000698739.1:n.2627T>G
ENST00000372371.8:c.2512T>G MANE Select	ENSP00000361446.3:p.Phe838Val
ENST00000372371.7:c.2512T>G	ENSP00000361446.3:p.Phe838Val
ENST00000472014.5:n.469+4631T>G
NM_007055.3:c.2512T>G	NP_008986.2:p.Phe838Val
NM_007055.4:c.2512T>G MANE Select	NP_008986.2:p.Phe838Val