Canonical Allele Identifier: CA377325978

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739923A>T (hg19) ; chr10:g.77980165A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980165A>T , CM000672.2:g.77980165A>T	GRCh38
NC_000010.10:g.79739923A>T , CM000672.1:g.79739923A>T	GRCh37
NC_000010.9:g.79409929A>T	NCBI36
NG_029648.1:g.54376T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1917T>A
ENST00000698725.1:n.1670T>A
ENST00000698726.1:n.3230T>A
ENST00000698727.1:n.2963T>A
ENST00000698728.1:n.3579T>A
ENST00000698729.1:n.5027T>A
ENST00000698730.1:n.5125T>A
ENST00000698731.1:c.3859T>A	ENSP00000513898.1:p.Phe1287Ile
ENST00000698732.1:c.*2689T>A	ENSP00000513899.1:n.*2689T>A
ENST00000698733.1:c.*3187T>A	ENSP00000513900.1:n.*3187T>A
ENST00000698734.1:c.*2173T>A	ENSP00000513901.1:n.*2173T>A
ENST00000698735.1:n.4351T>A
ENST00000698736.1:n.4764T>A
ENST00000698737.1:n.4115T>A
ENST00000372371.8:c.4000T>A MANE Select	ENSP00000361446.3:p.Phe1334Ile
ENST00000372371.7:c.4000T>A	ENSP00000361446.3:p.Phe1334Ile
ENST00000616246.4:c.448T>A	ENSP00000483738.1:p.Phe150Ile
NM_007055.3:c.4000T>A	NP_008986.2:p.Phe1334Ile
NM_007055.4:c.4000T>A MANE Select	NP_008986.2:p.Phe1334Ile