Canonical Allele Identifier: CA377325990

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739929C>T (hg19) ; chr10:g.77980171C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980171C>T , CM000672.2:g.77980171C>T	GRCh38
NC_000010.10:g.79739929C>T , CM000672.1:g.79739929C>T	GRCh37
NC_000010.9:g.79409935C>T	NCBI36
NG_029648.1:g.54370G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1911G>A
ENST00000698725.1:n.1664G>A
ENST00000698726.1:n.3224G>A
ENST00000698727.1:n.2957G>A
ENST00000698728.1:n.3573G>A
ENST00000698729.1:n.5021G>A
ENST00000698730.1:n.5119G>A
ENST00000698731.1:c.3853G>A	ENSP00000513898.1:p.Ala1285Thr
ENST00000698732.1:c.*2683G>A	ENSP00000513899.1:n.*2683G>A
ENST00000698733.1:c.*3181G>A	ENSP00000513900.1:n.*3181G>A
ENST00000698734.1:c.*2167G>A	ENSP00000513901.1:n.*2167G>A
ENST00000698735.1:n.4345G>A
ENST00000698736.1:n.4758G>A
ENST00000698737.1:n.4109G>A
ENST00000372371.8:c.3994G>A MANE Select	ENSP00000361446.3:p.Ala1332Thr
ENST00000372371.7:c.3994G>A	ENSP00000361446.3:p.Ala1332Thr
ENST00000616246.4:c.442G>A	ENSP00000483738.1:p.Ala148Thr
NM_007055.3:c.3994G>A	NP_008986.2:p.Ala1332Thr
NM_007055.4:c.3994G>A MANE Select	NP_008986.2:p.Ala1332Thr