Canonical Allele Identifier: CA2574591579
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77999972T>G , CM000672.2:g.77999972T>G GRCh38
NC_000010.10:g.79759730T>G , CM000672.1:g.79759730T>G GRCh37
NC_000010.9:g.79429736T>G NCBI36
NG_029648.1:g.34569A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698727.1:n.1676+9A>C
ENST00000698728.1:n.2195+9A>C
ENST00000698729.1:n.3741+9A>C
ENST00000698730.1:n.3741+9A>C
ENST00000698731.1:c.2475+9A>C ENSP00000513898.1:n.2475+9A>C
ENST00000698732.1:c.*1477+9A>C ENSP00000513899.1:n.*1477+9A>C
ENST00000698733.1:c.*1803+9A>C ENSP00000513900.1:n.*1803+9A>C
ENST00000698734.1:c.2616+9A>C ENSP00000513901.1:n.2616+9A>C
ENST00000698735.1:n.2731+9A>C
ENST00000698736.1:n.2731+9A>C
ENST00000698737.1:n.2731+9A>C
ENST00000698738.1:n.2731+9A>C
ENST00000698739.1:n.2731+9A>C
ENST00000372371.8:c.2616+9A>C MANE Select ENSP00000361446.3:n.2616+9A>C
ENST00000372371.7:c.2616+9A>C ENSP00000361446.3:n.2616+9A>C
ENST00000472014.5:n.469+4744A>C
NM_007055.3:c.2616+9A>C NP_008986.2:n.2616+9A>C
NM_007055.4:c.2616+9A>C MANE Select NP_008986.2:n.2616+9A>C