Canonical Allele Identifier: CA377326111

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739983T>G (hg19) ; chr10:g.77980225T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980225T>G , CM000672.2:g.77980225T>G	GRCh38
NC_000010.10:g.79739983T>G , CM000672.1:g.79739983T>G	GRCh37
NC_000010.9:g.79409989T>G	NCBI36
NG_029648.1:g.54316A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1857A>C
ENST00000698725.1:n.1610A>C
ENST00000698726.1:n.3170A>C
ENST00000698727.1:n.2903A>C
ENST00000698728.1:n.3519A>C
ENST00000698729.1:n.4967A>C
ENST00000698730.1:n.5065A>C
ENST00000698731.1:c.3799A>C	ENSP00000513898.1:p.Ser1267Arg
ENST00000698732.1:c.*2629A>C	ENSP00000513899.1:n.*2629A>C
ENST00000698733.1:c.*3127A>C	ENSP00000513900.1:n.*3127A>C
ENST00000698734.1:c.*2113A>C	ENSP00000513901.1:n.*2113A>C
ENST00000698735.1:n.4291A>C
ENST00000698736.1:n.4704A>C
ENST00000698737.1:n.4055A>C
ENST00000372371.8:c.3940A>C MANE Select	ENSP00000361446.3:p.Ser1314Arg
ENST00000372371.7:c.3940A>C	ENSP00000361446.3:p.Ser1314Arg
ENST00000616246.4:c.388A>C	ENSP00000483738.1:p.Ser130Arg
NM_007055.3:c.3940A>C	NP_008986.2:p.Ser1314Arg
NM_007055.4:c.3940A>C MANE Select	NP_008986.2:p.Ser1314Arg