Canonical Allele Identifier: CA377326012

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739938A>T (hg19) ; chr10:g.77980180A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980180A>T , CM000672.2:g.77980180A>T	GRCh38
NC_000010.10:g.79739938A>T , CM000672.1:g.79739938A>T	GRCh37
NC_000010.9:g.79409944A>T	NCBI36
NG_029648.1:g.54361T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1902T>A
ENST00000698725.1:n.1655T>A
ENST00000698726.1:n.3215T>A
ENST00000698727.1:n.2948T>A
ENST00000698728.1:n.3564T>A
ENST00000698729.1:n.5012T>A
ENST00000698730.1:n.5110T>A
ENST00000698731.1:c.3844T>A	ENSP00000513898.1:p.Phe1282Ile
ENST00000698732.1:c.*2674T>A	ENSP00000513899.1:n.*2674T>A
ENST00000698733.1:c.*3172T>A	ENSP00000513900.1:n.*3172T>A
ENST00000698734.1:c.*2158T>A	ENSP00000513901.1:n.*2158T>A
ENST00000698735.1:n.4336T>A
ENST00000698736.1:n.4749T>A
ENST00000698737.1:n.4100T>A
ENST00000372371.8:c.3985T>A MANE Select	ENSP00000361446.3:p.Phe1329Ile
ENST00000372371.7:c.3985T>A	ENSP00000361446.3:p.Phe1329Ile
ENST00000616246.4:c.433T>A	ENSP00000483738.1:p.Phe145Ile
NM_007055.3:c.3985T>A	NP_008986.2:p.Phe1329Ile
NM_007055.4:c.3985T>A MANE Select	NP_008986.2:p.Phe1329Ile