Canonical Allele Identifier: CA377326035

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739949G>T (hg19) ; chr10:g.77980191G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980191G>T , CM000672.2:g.77980191G>T	GRCh38
NC_000010.10:g.79739949G>T , CM000672.1:g.79739949G>T	GRCh37
NC_000010.9:g.79409955G>T	NCBI36
NG_029648.1:g.54350C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1891C>A
ENST00000698725.1:n.1644C>A
ENST00000698726.1:n.3204C>A
ENST00000698727.1:n.2937C>A
ENST00000698728.1:n.3553C>A
ENST00000698729.1:n.5001C>A
ENST00000698730.1:n.5099C>A
ENST00000698731.1:c.3833C>A	ENSP00000513898.1:p.Ala1278Asp
ENST00000698732.1:c.*2663C>A	ENSP00000513899.1:n.*2663C>A
ENST00000698733.1:c.*3161C>A	ENSP00000513900.1:n.*3161C>A
ENST00000698734.1:c.*2147C>A	ENSP00000513901.1:n.*2147C>A
ENST00000698735.1:n.4325C>A
ENST00000698736.1:n.4738C>A
ENST00000698737.1:n.4089C>A
ENST00000372371.8:c.3974C>A MANE Select	ENSP00000361446.3:p.Ala1325Asp
ENST00000372371.7:c.3974C>A	ENSP00000361446.3:p.Ala1325Asp
ENST00000616246.4:c.422C>A	ENSP00000483738.1:p.Ala141Asp
NM_007055.3:c.3974C>A	NP_008986.2:p.Ala1325Asp
NM_007055.4:c.3974C>A MANE Select	NP_008986.2:p.Ala1325Asp