Canonical Allele Identifier: CA377325960

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739915C>G (hg19) ; chr10:g.77980157C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980157C>G , CM000672.2:g.77980157C>G	GRCh38
NC_000010.10:g.79739915C>G , CM000672.1:g.79739915C>G	GRCh37
NC_000010.9:g.79409921C>G	NCBI36
NG_029648.1:g.54384G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1925G>C
ENST00000698725.1:n.1678G>C
ENST00000698726.1:n.3238G>C
ENST00000698727.1:n.2971G>C
ENST00000698728.1:n.3587G>C
ENST00000698729.1:n.5035G>C
ENST00000698730.1:n.5133G>C
ENST00000698731.1:c.3867G>C	ENSP00000513898.1:p.Gln1289His
ENST00000698732.1:c.*2697G>C	ENSP00000513899.1:n.*2697G>C
ENST00000698733.1:c.*3195G>C	ENSP00000513900.1:n.*3195G>C
ENST00000698734.1:c.*2181G>C	ENSP00000513901.1:n.*2181G>C
ENST00000698735.1:n.4359G>C
ENST00000698736.1:n.4772G>C
ENST00000698737.1:n.4123G>C
ENST00000372371.8:c.4008G>C MANE Select	ENSP00000361446.3:p.Gln1336His
ENST00000372371.7:c.4008G>C	ENSP00000361446.3:p.Gln1336His
ENST00000616246.4:c.456G>C	ENSP00000483738.1:p.Gln152His
NM_007055.3:c.4008G>C	NP_008986.2:p.Gln1336His
NM_007055.4:c.4008G>C MANE Select	NP_008986.2:p.Gln1336His