Canonical Allele Identifier: CA377326082
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980212A>G , CM000672.2:g.77980212A>G GRCh38
NC_000010.10:g.79739970A>G , CM000672.1:g.79739970A>G GRCh37
NC_000010.9:g.79409976A>G NCBI36
NG_029648.1:g.54329T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1870T>C
ENST00000698725.1:n.1623T>C
ENST00000698726.1:n.3183T>C
ENST00000698727.1:n.2916T>C
ENST00000698728.1:n.3532T>C
ENST00000698729.1:n.4980T>C
ENST00000698730.1:n.5078T>C
ENST00000698731.1:c.3812T>C ENSP00000513898.1:p.Leu1271Pro
ENST00000698732.1:c.*2642T>C ENSP00000513899.1:n.*2642T>C
ENST00000698733.1:c.*3140T>C ENSP00000513900.1:n.*3140T>C
ENST00000698734.1:c.*2126T>C ENSP00000513901.1:n.*2126T>C
ENST00000698735.1:n.4304T>C
ENST00000698736.1:n.4717T>C
ENST00000698737.1:n.4068T>C
ENST00000372371.8:c.3953T>C MANE Select ENSP00000361446.3:p.Leu1318Pro
ENST00000372371.7:c.3953T>C ENSP00000361446.3:p.Leu1318Pro
ENST00000616246.4:c.401T>C ENSP00000483738.1:p.Leu134Pro
NM_007055.3:c.3953T>C NP_008986.2:p.Leu1318Pro
NM_007055.4:c.3953T>C MANE Select NP_008986.2:p.Leu1318Pro