Canonical Allele Identifier: CA377326004

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739935C>A (hg19) ; chr10:g.77980177C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980177C>A , CM000672.2:g.77980177C>A	GRCh38
NC_000010.10:g.79739935C>A , CM000672.1:g.79739935C>A	GRCh37
NC_000010.9:g.79409941C>A	NCBI36
NG_029648.1:g.54364G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1905G>T
ENST00000698725.1:n.1658G>T
ENST00000698726.1:n.3218G>T
ENST00000698727.1:n.2951G>T
ENST00000698728.1:n.3567G>T
ENST00000698729.1:n.5015G>T
ENST00000698730.1:n.5113G>T
ENST00000698731.1:c.3847G>T	ENSP00000513898.1:p.Asp1283Tyr
ENST00000698732.1:c.*2677G>T	ENSP00000513899.1:n.*2677G>T
ENST00000698733.1:c.*3175G>T	ENSP00000513900.1:n.*3175G>T
ENST00000698734.1:c.*2161G>T	ENSP00000513901.1:n.*2161G>T
ENST00000698735.1:n.4339G>T
ENST00000698736.1:n.4752G>T
ENST00000698737.1:n.4103G>T
ENST00000372371.8:c.3988G>T MANE Select	ENSP00000361446.3:p.Asp1330Tyr
ENST00000372371.7:c.3988G>T	ENSP00000361446.3:p.Asp1330Tyr
ENST00000616246.4:c.436G>T	ENSP00000483738.1:p.Asp146Tyr
NM_007055.3:c.3988G>T	NP_008986.2:p.Asp1330Tyr
NM_007055.4:c.3988G>T MANE Select	NP_008986.2:p.Asp1330Tyr