Canonical Allele Identifier: CA377341057

Gene: POLR3A

Linked Data

• dbSNP Id: rs1847450182
• MyVariant Identifiers: chr10:g.79769698C>T (hg19) ; chr10:g.78009940C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009940C>T , CM000672.2:g.78009940C>T	GRCh38
NC_000010.10:g.79769698C>T , CM000672.1:g.79769698C>T	GRCh37
NC_000010.9:g.79439704C>T	NCBI36
NG_029648.1:g.24601G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698728.1:n.1273G>A
ENST00000698729.1:n.2819G>A
ENST00000698730.1:n.2819G>A
ENST00000698731.1:c.1553G>A	ENSP00000513898.1:p.Cys518Tyr
ENST00000698732.1:c.*555G>A	ENSP00000513899.1:n.*555G>A
ENST00000698733.1:c.*881G>A	ENSP00000513900.1:n.*881G>A
ENST00000698734.1:c.1694G>A	ENSP00000513901.1:p.Cys565Tyr
ENST00000698735.1:n.1809G>A
ENST00000698736.1:n.1809G>A
ENST00000698737.1:n.1809G>A
ENST00000698738.1:n.1809G>A
ENST00000698739.1:n.1809G>A
ENST00000372371.8:c.1694G>A MANE Select	ENSP00000361446.3:p.Cys565Tyr
ENST00000372371.7:c.1694G>A	ENSP00000361446.3:p.Cys565Tyr
ENST00000473588.2:c.496G>A
NM_007055.3:c.1694G>A	NP_008986.2:p.Cys565Tyr
NM_007055.4:c.1694G>A MANE Select	NP_008986.2:p.Cys565Tyr