Canonical Allele Identifier: CA377340946

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769647C>G (hg19) ; chr10:g.78009889C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009889C>G , CM000672.2:g.78009889C>G	GRCh38
NC_000010.10:g.79769647C>G , CM000672.1:g.79769647C>G	GRCh37
NC_000010.9:g.79439653C>G	NCBI36
NG_029648.1:g.24652G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698728.1:n.1324G>C
ENST00000698729.1:n.2870G>C
ENST00000698730.1:n.2870G>C
ENST00000698731.1:c.1604G>C	ENSP00000513898.1:p.Arg535Pro
ENST00000698732.1:c.*606G>C	ENSP00000513899.1:n.*606G>C
ENST00000698733.1:c.*932G>C	ENSP00000513900.1:n.*932G>C
ENST00000698734.1:c.1745G>C	ENSP00000513901.1:p.Arg582Pro
ENST00000698735.1:n.1860G>C
ENST00000698736.1:n.1860G>C
ENST00000698737.1:n.1860G>C
ENST00000698738.1:n.1860G>C
ENST00000698739.1:n.1860G>C
ENST00000372371.8:c.1745G>C MANE Select	ENSP00000361446.3:p.Arg582Pro
ENST00000372371.7:c.1745G>C	ENSP00000361446.3:p.Arg582Pro
ENST00000473588.2:c.547G>C
NM_007055.3:c.1745G>C	NP_008986.2:p.Arg582Pro
NM_007055.4:c.1745G>C MANE Select	NP_008986.2:p.Arg582Pro