Canonical Allele Identifier: CA377335569

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759813A>C (hg19) ; chr10:g.78000055A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000055A>C , CM000672.2:g.78000055A>C	GRCh38
NC_000010.10:g.79759813A>C , CM000672.1:g.79759813A>C	GRCh37
NC_000010.9:g.79429819A>C	NCBI36
NG_029648.1:g.34486T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698727.1:n.1602T>G
ENST00000698728.1:n.2121T>G
ENST00000698729.1:n.3667T>G
ENST00000698730.1:n.3667T>G
ENST00000698731.1:c.2401T>G	ENSP00000513898.1:p.Phe801Val
ENST00000698732.1:c.*1403T>G	ENSP00000513899.1:n.*1403T>G
ENST00000698733.1:c.*1729T>G	ENSP00000513900.1:n.*1729T>G
ENST00000698734.1:c.2542T>G	ENSP00000513901.1:p.Phe848Val
ENST00000698735.1:n.2657T>G
ENST00000698736.1:n.2657T>G
ENST00000698737.1:n.2657T>G
ENST00000698738.1:n.2657T>G
ENST00000698739.1:n.2657T>G
ENST00000372371.8:c.2542T>G MANE Select	ENSP00000361446.3:p.Phe848Val
ENST00000372371.7:c.2542T>G	ENSP00000361446.3:p.Phe848Val
ENST00000472014.5:n.469+4661T>G
NM_007055.3:c.2542T>G	NP_008986.2:p.Phe848Val
NM_007055.4:c.2542T>G MANE Select	NP_008986.2:p.Phe848Val