Canonical Allele Identifier: CA470397163

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759802T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000044T>A , CM000672.2:g.78000044T>A	GRCh38
NC_000010.10:g.79759802T>A , CM000672.1:g.79759802T>A	GRCh37
NC_000010.9:g.79429808T>A	NCBI36
NG_029648.1:g.34497A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698727.1:n.1613A>T
ENST00000698728.1:n.2132A>T
ENST00000698729.1:n.3678A>T
ENST00000698730.1:n.3678A>T
ENST00000698731.1:c.2412A>T	ENSP00000513898.1:p.Thr804=
ENST00000698732.1:c.*1414A>T	ENSP00000513899.1:n.*1414A>T
ENST00000698733.1:c.*1740A>T	ENSP00000513900.1:n.*1740A>T
ENST00000698734.1:c.2553A>T	ENSP00000513901.1:p.Thr851=
ENST00000698735.1:n.2668A>T
ENST00000698736.1:n.2668A>T
ENST00000698737.1:n.2668A>T
ENST00000698738.1:n.2668A>T
ENST00000698739.1:n.2668A>T
ENST00000372371.8:c.2553A>T MANE Select	ENSP00000361446.3:p.Thr851=
ENST00000372371.7:c.2553A>T	ENSP00000361446.3:p.Thr851=
ENST00000472014.5:n.469+4672A>T
NM_007055.3:c.2553A>T	NP_008986.2:p.Thr851=
NM_007055.4:c.2553A>T MANE Select	NP_008986.2:p.Thr851=