Canonical Allele Identifier: CA377325988

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739928G>C (hg19) ; chr10:g.77980170G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980170G>C , CM000672.2:g.77980170G>C	GRCh38
NC_000010.10:g.79739928G>C , CM000672.1:g.79739928G>C	GRCh37
NC_000010.9:g.79409934G>C	NCBI36
NG_029648.1:g.54371C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1912C>G
ENST00000698725.1:n.1665C>G
ENST00000698726.1:n.3225C>G
ENST00000698727.1:n.2958C>G
ENST00000698728.1:n.3574C>G
ENST00000698729.1:n.5022C>G
ENST00000698730.1:n.5120C>G
ENST00000698731.1:c.3854C>G	ENSP00000513898.1:p.Ala1285Gly
ENST00000698732.1:c.*2684C>G	ENSP00000513899.1:n.*2684C>G
ENST00000698733.1:c.*3182C>G	ENSP00000513900.1:n.*3182C>G
ENST00000698734.1:c.*2168C>G	ENSP00000513901.1:n.*2168C>G
ENST00000698735.1:n.4346C>G
ENST00000698736.1:n.4759C>G
ENST00000698737.1:n.4110C>G
ENST00000372371.8:c.3995C>G MANE Select	ENSP00000361446.3:p.Ala1332Gly
ENST00000372371.7:c.3995C>G	ENSP00000361446.3:p.Ala1332Gly
ENST00000616246.4:c.443C>G	ENSP00000483738.1:p.Ala148Gly
NM_007055.3:c.3995C>G	NP_008986.2:p.Ala1332Gly
NM_007055.4:c.3995C>G MANE Select	NP_008986.2:p.Ala1332Gly