Canonical Allele Identifier: CA377337957

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79764503G>A (hg19) ; chr10:g.78004745G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78004745G>A , CM000672.2:g.78004745G>A	GRCh38
NC_000010.10:g.79764503G>A , CM000672.1:g.79764503G>A	GRCh37
NC_000010.9:g.79434509G>A	NCBI36
NG_029648.1:g.29796C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1278C>T
ENST00000698728.1:n.1797C>T
ENST00000698729.1:n.3343C>T
ENST00000698730.1:n.3343C>T
ENST00000698731.1:c.2077C>T	ENSP00000513898.1:p.Pro693Ser
ENST00000698732.1:c.*1079C>T	ENSP00000513899.1:n.*1079C>T
ENST00000698733.1:c.*1405C>T	ENSP00000513900.1:n.*1405C>T
ENST00000698734.1:c.2218C>T	ENSP00000513901.1:p.Pro740Ser
ENST00000698735.1:n.2333C>T
ENST00000698736.1:n.2333C>T
ENST00000698737.1:n.2333C>T
ENST00000698738.1:n.2333C>T
ENST00000698739.1:n.2333C>T
ENST00000372371.8:c.2218C>T MANE Select	ENSP00000361446.3:p.Pro740Ser
ENST00000372371.7:c.2218C>T	ENSP00000361446.3:p.Pro740Ser
ENST00000472014.5:n.440C>T
ENST00000473588.2:c.881C>T
NM_007055.3:c.2218C>T	NP_008986.2:p.Pro740Ser
NM_007055.4:c.2218C>T MANE Select	NP_008986.2:p.Pro740Ser