Canonical Allele Identifier: CA377326091
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980215A>T , CM000672.2:g.77980215A>T GRCh38
NC_000010.10:g.79739973A>T , CM000672.1:g.79739973A>T GRCh37
NC_000010.9:g.79409979A>T NCBI36
NG_029648.1:g.54326T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1867T>A
ENST00000698725.1:n.1620T>A
ENST00000698726.1:n.3180T>A
ENST00000698727.1:n.2913T>A
ENST00000698728.1:n.3529T>A
ENST00000698729.1:n.4977T>A
ENST00000698730.1:n.5075T>A
ENST00000698731.1:c.3809T>A ENSP00000513898.1:p.Met1270Lys
ENST00000698732.1:c.*2639T>A ENSP00000513899.1:n.*2639T>A
ENST00000698733.1:c.*3137T>A ENSP00000513900.1:n.*3137T>A
ENST00000698734.1:c.*2123T>A ENSP00000513901.1:n.*2123T>A
ENST00000698735.1:n.4301T>A
ENST00000698736.1:n.4714T>A
ENST00000698737.1:n.4065T>A
ENST00000372371.8:c.3950T>A MANE Select ENSP00000361446.3:p.Met1317Lys
ENST00000372371.7:c.3950T>A ENSP00000361446.3:p.Met1317Lys
ENST00000616246.4:c.398T>A ENSP00000483738.1:p.Met133Lys
NM_007055.3:c.3950T>A NP_008986.2:p.Met1317Lys
NM_007055.4:c.3950T>A MANE Select NP_008986.2:p.Met1317Lys