Canonical Allele Identifier: CA377326089

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739973A>C (hg19) ; chr10:g.77980215A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980215A>C , CM000672.2:g.77980215A>C	GRCh38
NC_000010.10:g.79739973A>C , CM000672.1:g.79739973A>C	GRCh37
NC_000010.9:g.79409979A>C	NCBI36
NG_029648.1:g.54326T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1867T>G
ENST00000698725.1:n.1620T>G
ENST00000698726.1:n.3180T>G
ENST00000698727.1:n.2913T>G
ENST00000698728.1:n.3529T>G
ENST00000698729.1:n.4977T>G
ENST00000698730.1:n.5075T>G
ENST00000698731.1:c.3809T>G	ENSP00000513898.1:p.Met1270Arg
ENST00000698732.1:c.*2639T>G	ENSP00000513899.1:n.*2639T>G
ENST00000698733.1:c.*3137T>G	ENSP00000513900.1:n.*3137T>G
ENST00000698734.1:c.*2123T>G	ENSP00000513901.1:n.*2123T>G
ENST00000698735.1:n.4301T>G
ENST00000698736.1:n.4714T>G
ENST00000698737.1:n.4065T>G
ENST00000372371.8:c.3950T>G MANE Select	ENSP00000361446.3:p.Met1317Arg
ENST00000372371.7:c.3950T>G	ENSP00000361446.3:p.Met1317Arg
ENST00000616246.4:c.398T>G	ENSP00000483738.1:p.Met133Arg
NM_007055.3:c.3950T>G	NP_008986.2:p.Met1317Arg
NM_007055.4:c.3950T>G MANE Select	NP_008986.2:p.Met1317Arg