Canonical Allele Identifier: CA377333998

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79752993C>G (hg19) ; chr10:g.77993235C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77993235C>G , CM000672.2:g.77993235C>G	GRCh38
NC_000010.10:g.79752993C>G , CM000672.1:g.79752993C>G	GRCh37
NC_000010.9:g.79422999C>G	NCBI36
NG_029648.1:g.41306G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.17G>C
ENST00000698727.1:n.1809G>C
ENST00000698728.1:n.2328G>C
ENST00000698729.1:n.3874G>C
ENST00000698730.1:n.3874G>C
ENST00000698731.1:c.2608G>C	ENSP00000513898.1:p.Glu870Gln
ENST00000698732.1:c.*1610G>C	ENSP00000513899.1:n.*1610G>C
ENST00000698733.1:c.*1936G>C	ENSP00000513900.1:n.*1936G>C
ENST00000698734.1:c.*273G>C	ENSP00000513901.1:n.*273G>C
ENST00000698735.1:n.2864G>C
ENST00000698736.1:n.2864G>C
ENST00000698737.1:n.2864G>C
ENST00000698738.1:n.2864G>C
ENST00000698739.1:n.2864G>C
ENST00000372371.8:c.2749G>C MANE Select	ENSP00000361446.3:p.Glu917Gln
ENST00000372371.7:c.2749G>C	ENSP00000361446.3:p.Glu917Gln
ENST00000472014.5:n.602G>C
NM_007055.3:c.2749G>C	NP_008986.2:p.Glu917Gln
NM_007055.4:c.2749G>C MANE Select	NP_008986.2:p.Glu917Gln