Canonical Allele Identifier: CA377325926
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980143C>A , CM000672.2:g.77980143C>A GRCh38
NC_000010.10:g.79739901C>A , CM000672.1:g.79739901C>A GRCh37
NC_000010.9:g.79409907C>A NCBI36
NG_029648.1:g.54398G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1939G>T
ENST00000698725.1:n.1692G>T
ENST00000698726.1:n.3252G>T
ENST00000698727.1:n.2985G>T
ENST00000698728.1:n.3601G>T
ENST00000698729.1:n.5049G>T
ENST00000698730.1:n.5147G>T
ENST00000698731.1:c.3881G>T ENSP00000513898.1:p.Cys1294Phe
ENST00000698732.1:c.*2711G>T ENSP00000513899.1:n.*2711G>T
ENST00000698733.1:c.*3209G>T ENSP00000513900.1:n.*3209G>T
ENST00000698734.1:c.*2195G>T ENSP00000513901.1:n.*2195G>T
ENST00000698735.1:n.4373G>T
ENST00000698736.1:n.4786G>T
ENST00000698737.1:n.4137G>T
ENST00000372371.8:c.4022G>T MANE Select ENSP00000361446.3:p.Cys1341Phe
ENST00000372371.7:c.4022G>T ENSP00000361446.3:p.Cys1341Phe
ENST00000616246.4:c.470G>T ENSP00000483738.1:p.Cys157Phe
NM_007055.3:c.4022G>T NP_008986.2:p.Cys1341Phe
NM_007055.4:c.4022G>T MANE Select NP_008986.2:p.Cys1341Phe