Canonical Allele Identifier: CA2609821160
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980133A>G , CM000672.2:g.77980133A>G GRCh38
NC_000010.10:g.79739891A>G , CM000672.1:g.79739891A>G GRCh37
NC_000010.9:g.79409897A>G NCBI36
NG_029648.1:g.54408T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1941+8T>C
ENST00000698725.1:n.1694+8T>C
ENST00000698726.1:n.3254+8T>C
ENST00000698727.1:n.2987+8T>C
ENST00000698728.1:n.3603+8T>C
ENST00000698729.1:n.5051+8T>C
ENST00000698730.1:n.5149+8T>C
ENST00000698731.1:c.3883+8T>C ENSP00000513898.1:n.3883+8T>C
ENST00000698732.1:c.*2713+8T>C ENSP00000513899.1:n.*2713+8T>C
ENST00000698733.1:c.*3211+8T>C ENSP00000513900.1:n.*3211+8T>C
ENST00000698734.1:c.*2197+8T>C ENSP00000513901.1:n.*2197+8T>C
ENST00000698735.1:n.4375+8T>C
ENST00000698736.1:n.4788+8T>C
ENST00000698737.1:n.4147T>C
ENST00000372371.8:c.4024+8T>C MANE Select ENSP00000361446.3:n.4024+8T>C
ENST00000372371.7:c.4024+8T>C ENSP00000361446.3:n.4024+8T>C
ENST00000616246.4:c.472+8T>C ENSP00000483738.1:n.472+8T>C
NM_007055.3:c.4024+8T>C NP_008986.2:n.4024+8T>C
NM_007055.4:c.4024+8T>C MANE Select NP_008986.2:n.4024+8T>C