Canonical Allele Identifier: CA470390671

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739996G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980238G>A , CM000672.2:g.77980238G>A	GRCh38
NC_000010.10:g.79739996G>A , CM000672.1:g.79739996G>A	GRCh37
NC_000010.9:g.79410002G>A	NCBI36
NG_029648.1:g.54303C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1844C>T
ENST00000698725.1:n.1597C>T
ENST00000698726.1:n.3157C>T
ENST00000698727.1:n.2890C>T
ENST00000698728.1:n.3506C>T
ENST00000698729.1:n.4954C>T
ENST00000698730.1:n.5052C>T
ENST00000698731.1:c.3786C>T	ENSP00000513898.1:p.Ala1262=
ENST00000698732.1:c.*2616C>T	ENSP00000513899.1:n.*2616C>T
ENST00000698733.1:c.*3114C>T	ENSP00000513900.1:n.*3114C>T
ENST00000698734.1:c.*2100C>T	ENSP00000513901.1:n.*2100C>T
ENST00000698735.1:n.4278C>T
ENST00000698736.1:n.4691C>T
ENST00000698737.1:n.4042C>T
ENST00000372371.8:c.3927C>T MANE Select	ENSP00000361446.3:p.Ala1309=
ENST00000372371.7:c.3927C>T	ENSP00000361446.3:p.Ala1309=
ENST00000616246.4:c.375C>T	ENSP00000483738.1:p.Ala125=
NM_007055.3:c.3927C>T	NP_008986.2:p.Ala1309=
NM_007055.4:c.3927C>T MANE Select	NP_008986.2:p.Ala1309=