Canonical Allele Identifier: CA470397631

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79764549A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78004791A>G , CM000672.2:g.78004791A>G	GRCh38
NC_000010.10:g.79764549A>G , CM000672.1:g.79764549A>G	GRCh37
NC_000010.9:g.79434555A>G	NCBI36
NG_029648.1:g.29750T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1232T>C
ENST00000698728.1:n.1751T>C
ENST00000698729.1:n.3297T>C
ENST00000698730.1:n.3297T>C
ENST00000698731.1:c.2031T>C	ENSP00000513898.1:p.Cys677=
ENST00000698732.1:c.*1033T>C	ENSP00000513899.1:n.*1033T>C
ENST00000698733.1:c.*1359T>C	ENSP00000513900.1:n.*1359T>C
ENST00000698734.1:c.2172T>C	ENSP00000513901.1:p.Cys724=
ENST00000698735.1:n.2287T>C
ENST00000698736.1:n.2287T>C
ENST00000698737.1:n.2287T>C
ENST00000698738.1:n.2287T>C
ENST00000698739.1:n.2287T>C
ENST00000372371.8:c.2172T>C MANE Select	ENSP00000361446.3:p.Cys724=
ENST00000372371.7:c.2172T>C	ENSP00000361446.3:p.Cys724=
ENST00000472014.5:n.394T>C
ENST00000473588.2:c.835T>C
NM_007055.3:c.2172T>C	NP_008986.2:p.Cys724=
NM_007055.4:c.2172T>C MANE Select	NP_008986.2:p.Cys724=