Canonical Allele Identifier: CA377340903

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769623T>C (hg19) ; chr10:g.78009865T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009865T>C , CM000672.2:g.78009865T>C	GRCh38
NC_000010.10:g.79769623T>C , CM000672.1:g.79769623T>C	GRCh37
NC_000010.9:g.79439629T>C	NCBI36
NG_029648.1:g.24676A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698728.1:n.1348A>G
ENST00000698729.1:n.2894A>G
ENST00000698730.1:n.2894A>G
ENST00000698731.1:c.1628A>G	ENSP00000513898.1:p.Lys543Arg
ENST00000698732.1:c.*630A>G	ENSP00000513899.1:n.*630A>G
ENST00000698733.1:c.*956A>G	ENSP00000513900.1:n.*956A>G
ENST00000698734.1:c.1769A>G	ENSP00000513901.1:p.Lys590Arg
ENST00000698735.1:n.1884A>G
ENST00000698736.1:n.1884A>G
ENST00000698737.1:n.1884A>G
ENST00000698738.1:n.1884A>G
ENST00000698739.1:n.1884A>G
ENST00000372371.8:c.1769A>G MANE Select	ENSP00000361446.3:p.Lys590Arg
ENST00000372371.7:c.1769A>G	ENSP00000361446.3:p.Lys590Arg
ENST00000473588.2:c.571A>G
NM_007055.3:c.1769A>G	NP_008986.2:p.Lys590Arg
NM_007055.4:c.1769A>G MANE Select	NP_008986.2:p.Lys590Arg