Canonical Allele Identifier: CA470390633

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739927G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980169G>A , CM000672.2:g.77980169G>A	GRCh38
NC_000010.10:g.79739927G>A , CM000672.1:g.79739927G>A	GRCh37
NC_000010.9:g.79409933G>A	NCBI36
NG_029648.1:g.54372C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1913C>T
ENST00000698725.1:n.1666C>T
ENST00000698726.1:n.3226C>T
ENST00000698727.1:n.2959C>T
ENST00000698728.1:n.3575C>T
ENST00000698729.1:n.5023C>T
ENST00000698730.1:n.5121C>T
ENST00000698731.1:c.3855C>T	ENSP00000513898.1:p.Ala1285=
ENST00000698732.1:c.*2685C>T	ENSP00000513899.1:n.*2685C>T
ENST00000698733.1:c.*3183C>T	ENSP00000513900.1:n.*3183C>T
ENST00000698734.1:c.*2169C>T	ENSP00000513901.1:n.*2169C>T
ENST00000698735.1:n.4347C>T
ENST00000698736.1:n.4760C>T
ENST00000698737.1:n.4111C>T
ENST00000372371.8:c.3996C>T MANE Select	ENSP00000361446.3:p.Ala1332=
ENST00000372371.7:c.3996C>T	ENSP00000361446.3:p.Ala1332=
ENST00000616246.4:c.444C>T	ENSP00000483738.1:p.Ala148=
NM_007055.3:c.3996C>T	NP_008986.2:p.Ala1332=
NM_007055.4:c.3996C>T MANE Select	NP_008986.2:p.Ala1332=