Canonical Allele Identifier: CA1921507452
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78002138G= , CM000672.2:g.78002138G= GRCh38
NC_000010.10:g.79761896G= , CM000672.1:g.79761896G= GRCh37
NC_000010.9:g.79431902G= NCBI36
NG_029648.1:g.32403C=

Transcript Alleles

HGVS Amino-acid change
ENST00000698727.1:n.1419+59C=
ENST00000698728.1:n.1938+59C=
ENST00000698729.1:n.3484+59C=
ENST00000698730.1:n.3484+59C=
ENST00000698731.1:c.2218+59C= ENSP00000513898.1:n.2218+59C=
ENST00000698732.1:c.*1220+59C= ENSP00000513899.1:n.*1220+59C=
ENST00000698733.1:c.*1546+59C= ENSP00000513900.1:n.*1546+59C=
ENST00000698734.1:c.2359+59C= ENSP00000513901.1:n.2359+59C=
ENST00000698735.1:n.2474+59C=
ENST00000698736.1:n.2474+59C=
ENST00000698737.1:n.2474+59C=
ENST00000698738.1:n.2474+59C=
ENST00000698739.1:n.2474+59C=
ENST00000372371.8:c.2359+59C= MANE Select ENSP00000361446.3:n.2359+59C=
ENST00000372371.7:c.2359+59C= ENSP00000361446.3:n.2359+59C=
ENST00000472014.5:n.469+2578C=
NM_007055.3:c.2359+59C= NP_008986.2:n.2359+59C=
NM_007055.4:c.2359+59C= MANE Select NP_008986.2:n.2359+59C=