Canonical Allele Identifier: CA377340951

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769650A>C (hg19) ; chr10:g.78009892A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009892A>C , CM000672.2:g.78009892A>C	GRCh38
NC_000010.10:g.79769650A>C , CM000672.1:g.79769650A>C	GRCh37
NC_000010.9:g.79439656A>C	NCBI36
NG_029648.1:g.24649T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698728.1:n.1321T>G
ENST00000698729.1:n.2867T>G
ENST00000698730.1:n.2867T>G
ENST00000698731.1:c.1601T>G	ENSP00000513898.1:p.Val534Gly
ENST00000698732.1:c.*603T>G	ENSP00000513899.1:n.*603T>G
ENST00000698733.1:c.*929T>G	ENSP00000513900.1:n.*929T>G
ENST00000698734.1:c.1742T>G	ENSP00000513901.1:p.Val581Gly
ENST00000698735.1:n.1857T>G
ENST00000698736.1:n.1857T>G
ENST00000698737.1:n.1857T>G
ENST00000698738.1:n.1857T>G
ENST00000698739.1:n.1857T>G
ENST00000372371.8:c.1742T>G MANE Select	ENSP00000361446.3:p.Val581Gly
ENST00000372371.7:c.1742T>G	ENSP00000361446.3:p.Val581Gly
ENST00000473588.2:c.544T>G
NM_007055.3:c.1742T>G	NP_008986.2:p.Val581Gly
NM_007055.4:c.1742T>G MANE Select	NP_008986.2:p.Val581Gly