Canonical Allele Identifier: CA377326130

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739990C>G (hg19) ; chr10:g.77980232C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980232C>G , CM000672.2:g.77980232C>G	GRCh38
NC_000010.10:g.79739990C>G , CM000672.1:g.79739990C>G	GRCh37
NC_000010.9:g.79409996C>G	NCBI36
NG_029648.1:g.54309G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1850G>C
ENST00000698725.1:n.1603G>C
ENST00000698726.1:n.3163G>C
ENST00000698727.1:n.2896G>C
ENST00000698728.1:n.3512G>C
ENST00000698729.1:n.4960G>C
ENST00000698730.1:n.5058G>C
ENST00000698731.1:c.3792G>C	ENSP00000513898.1:p.Met1264Ile
ENST00000698732.1:c.*2622G>C	ENSP00000513899.1:n.*2622G>C
ENST00000698733.1:c.*3120G>C	ENSP00000513900.1:n.*3120G>C
ENST00000698734.1:c.*2106G>C	ENSP00000513901.1:n.*2106G>C
ENST00000698735.1:n.4284G>C
ENST00000698736.1:n.4697G>C
ENST00000698737.1:n.4048G>C
ENST00000372371.8:c.3933G>C MANE Select	ENSP00000361446.3:p.Met1311Ile
ENST00000372371.7:c.3933G>C	ENSP00000361446.3:p.Met1311Ile
ENST00000616246.4:c.381G>C	ENSP00000483738.1:p.Met127Ile
NM_007055.3:c.3933G>C	NP_008986.2:p.Met1311Ile
NM_007055.4:c.3933G>C MANE Select	NP_008986.2:p.Met1311Ile