Canonical Allele Identifier: CA1921508651
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78004698C= , CM000672.2:g.78004698C= GRCh38
NC_000010.10:g.79764456C= , CM000672.1:g.79764456C= GRCh37
NC_000010.9:g.79434462C= NCBI36
NG_029648.1:g.29843G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698727.1:n.1307+18G=
ENST00000698728.1:n.1826+18G=
ENST00000698729.1:n.3372+18G=
ENST00000698730.1:n.3372+18G=
ENST00000698731.1:c.2106+18G= ENSP00000513898.1:n.2106+18G=
ENST00000698732.1:c.*1108+18G= ENSP00000513899.1:n.*1108+18G=
ENST00000698733.1:c.*1434+18G= ENSP00000513900.1:n.*1434+18G=
ENST00000698734.1:c.2247+18G= ENSP00000513901.1:n.2247+18G=
ENST00000698735.1:n.2362+18G=
ENST00000698736.1:n.2362+18G=
ENST00000698737.1:n.2362+18G=
ENST00000698738.1:n.2362+18G=
ENST00000698739.1:n.2362+18G=
ENST00000372371.8:c.2247+18G= MANE Select ENSP00000361446.3:n.2247+18G=
ENST00000372371.7:c.2247+18G= ENSP00000361446.3:n.2247+18G=
ENST00000472014.5:n.469+18G=
ENST00000473588.2:c.910+18G=
NM_007055.3:c.2247+18G= NP_008986.2:n.2247+18G=
NM_007055.4:c.2247+18G= MANE Select NP_008986.2:n.2247+18G=