Canonical Allele Identifier: CA377337908

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79764494T>A (hg19) ; chr10:g.78004736T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78004736T>A , CM000672.2:g.78004736T>A	GRCh38
NC_000010.10:g.79764494T>A , CM000672.1:g.79764494T>A	GRCh37
NC_000010.9:g.79434500T>A	NCBI36
NG_029648.1:g.29805A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1287A>T
ENST00000698728.1:n.1806A>T
ENST00000698729.1:n.3352A>T
ENST00000698730.1:n.3352A>T
ENST00000698731.1:c.2086A>T	ENSP00000513898.1:p.Thr696Ser
ENST00000698732.1:c.*1088A>T	ENSP00000513899.1:n.*1088A>T
ENST00000698733.1:c.*1414A>T	ENSP00000513900.1:n.*1414A>T
ENST00000698734.1:c.2227A>T	ENSP00000513901.1:p.Thr743Ser
ENST00000698735.1:n.2342A>T
ENST00000698736.1:n.2342A>T
ENST00000698737.1:n.2342A>T
ENST00000698738.1:n.2342A>T
ENST00000698739.1:n.2342A>T
ENST00000372371.8:c.2227A>T MANE Select	ENSP00000361446.3:p.Thr743Ser
ENST00000372371.7:c.2227A>T	ENSP00000361446.3:p.Thr743Ser
ENST00000472014.5:n.449A>T
ENST00000473588.2:c.890A>T
NM_007055.3:c.2227A>T	NP_008986.2:p.Thr743Ser
NM_007055.4:c.2227A>T MANE Select	NP_008986.2:p.Thr743Ser