Canonical Allele Identifier: CA377340911

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769627G>C (hg19) ; chr10:g.78009869G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009869G>C , CM000672.2:g.78009869G>C	GRCh38
NC_000010.10:g.79769627G>C , CM000672.1:g.79769627G>C	GRCh37
NC_000010.9:g.79439633G>C	NCBI36
NG_029648.1:g.24672C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698728.1:n.1344C>G
ENST00000698729.1:n.2890C>G
ENST00000698730.1:n.2890C>G
ENST00000698731.1:c.1624C>G	ENSP00000513898.1:p.Leu542Val
ENST00000698732.1:c.*626C>G	ENSP00000513899.1:n.*626C>G
ENST00000698733.1:c.*952C>G	ENSP00000513900.1:n.*952C>G
ENST00000698734.1:c.1765C>G	ENSP00000513901.1:p.Leu589Val
ENST00000698735.1:n.1880C>G
ENST00000698736.1:n.1880C>G
ENST00000698737.1:n.1880C>G
ENST00000698738.1:n.1880C>G
ENST00000698739.1:n.1880C>G
ENST00000372371.8:c.1765C>G MANE Select	ENSP00000361446.3:p.Leu589Val
ENST00000372371.7:c.1765C>G	ENSP00000361446.3:p.Leu589Val
ENST00000473588.2:c.567C>G
NM_007055.3:c.1765C>G	NP_008986.2:p.Leu589Val
NM_007055.4:c.1765C>G MANE Select	NP_008986.2:p.Leu589Val