Canonical Allele Identifier: CA377325958

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739914T>G (hg19) ; chr10:g.77980156T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980156T>G , CM000672.2:g.77980156T>G	GRCh38
NC_000010.10:g.79739914T>G , CM000672.1:g.79739914T>G	GRCh37
NC_000010.9:g.79409920T>G	NCBI36
NG_029648.1:g.54385A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1926A>C
ENST00000698725.1:n.1679A>C
ENST00000698726.1:n.3239A>C
ENST00000698727.1:n.2972A>C
ENST00000698728.1:n.3588A>C
ENST00000698729.1:n.5036A>C
ENST00000698730.1:n.5134A>C
ENST00000698731.1:c.3868A>C	ENSP00000513898.1:p.Lys1290Gln
ENST00000698732.1:c.*2698A>C	ENSP00000513899.1:n.*2698A>C
ENST00000698733.1:c.*3196A>C	ENSP00000513900.1:n.*3196A>C
ENST00000698734.1:c.*2182A>C	ENSP00000513901.1:n.*2182A>C
ENST00000698735.1:n.4360A>C
ENST00000698736.1:n.4773A>C
ENST00000698737.1:n.4124A>C
ENST00000372371.8:c.4009A>C MANE Select	ENSP00000361446.3:p.Lys1337Gln
ENST00000372371.7:c.4009A>C	ENSP00000361446.3:p.Lys1337Gln
ENST00000616246.4:c.457A>C	ENSP00000483738.1:p.Lys153Gln
NM_007055.3:c.4009A>C	NP_008986.2:p.Lys1337Gln
NM_007055.4:c.4009A>C MANE Select	NP_008986.2:p.Lys1337Gln