Canonical Allele Identifier: CA377326176

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79740012G>A (hg19) ; chr10:g.77980254G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980254G>A , CM000672.2:g.77980254G>A	GRCh38
NC_000010.10:g.79740012G>A , CM000672.1:g.79740012G>A	GRCh37
NC_000010.9:g.79410018G>A	NCBI36
NG_029648.1:g.54287C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1828C>T
ENST00000698725.1:n.1581C>T
ENST00000698726.1:n.3141C>T
ENST00000698727.1:n.2874C>T
ENST00000698728.1:n.3490C>T
ENST00000698729.1:n.4938C>T
ENST00000698730.1:n.5036C>T
ENST00000698731.1:c.3770C>T	ENSP00000513898.1:p.Thr1257Ile
ENST00000698732.1:c.*2600C>T	ENSP00000513899.1:n.*2600C>T
ENST00000698733.1:c.*3098C>T	ENSP00000513900.1:n.*3098C>T
ENST00000698734.1:c.*2084C>T	ENSP00000513901.1:n.*2084C>T
ENST00000698735.1:n.4262C>T
ENST00000698736.1:n.4675C>T
ENST00000698737.1:n.4026C>T
ENST00000372371.8:c.3911C>T MANE Select	ENSP00000361446.3:p.Thr1304Ile
ENST00000372371.7:c.3911C>T	ENSP00000361446.3:p.Thr1304Ile
ENST00000616246.4:c.359C>T	ENSP00000483738.1:p.Thr120Ile
NM_007055.3:c.3911C>T	NP_008986.2:p.Thr1304Ile
NM_007055.4:c.3911C>T MANE Select	NP_008986.2:p.Thr1304Ile