Canonical Allele Identifier: CA377326210

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79740024A>G (hg19) ; chr10:g.77980266A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980266A>G , CM000672.2:g.77980266A>G	GRCh38
NC_000010.10:g.79740024A>G , CM000672.1:g.79740024A>G	GRCh37
NC_000010.9:g.79410030A>G	NCBI36
NG_029648.1:g.54275T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1816T>C
ENST00000698725.1:n.1569T>C
ENST00000698726.1:n.3129T>C
ENST00000698727.1:n.2862T>C
ENST00000698728.1:n.3478T>C
ENST00000698729.1:n.4926T>C
ENST00000698730.1:n.5024T>C
ENST00000698731.1:c.3758T>C	ENSP00000513898.1:p.Val1253Ala
ENST00000698732.1:c.*2588T>C	ENSP00000513899.1:n.*2588T>C
ENST00000698733.1:c.*3086T>C	ENSP00000513900.1:n.*3086T>C
ENST00000698734.1:c.*2072T>C	ENSP00000513901.1:n.*2072T>C
ENST00000698735.1:n.4250T>C
ENST00000698736.1:n.4663T>C
ENST00000698737.1:n.4014T>C
ENST00000372371.8:c.3899T>C MANE Select	ENSP00000361446.3:p.Val1300Ala
ENST00000372371.7:c.3899T>C	ENSP00000361446.3:p.Val1300Ala
ENST00000616246.4:c.347T>C	ENSP00000483738.1:p.Val116Ala
NM_007055.3:c.3899T>C	NP_008986.2:p.Val1300Ala
NM_007055.4:c.3899T>C MANE Select	NP_008986.2:p.Val1300Ala