Canonical Allele Identifier: CA377333996
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77993235C>A , CM000672.2:g.77993235C>A GRCh38
NC_000010.10:g.79752993C>A , CM000672.1:g.79752993C>A GRCh37
NC_000010.9:g.79422999C>A NCBI36
NG_029648.1:g.41306G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698724.1:n.17G>T
ENST00000698727.1:n.1809G>T
ENST00000698728.1:n.2328G>T
ENST00000698729.1:n.3874G>T
ENST00000698730.1:n.3874G>T
ENST00000698731.1:c.2608G>T ENSP00000513898.1:p.Glu870Ter
ENST00000698732.1:c.*1610G>T ENSP00000513899.1:n.*1610G>T
ENST00000698733.1:c.*1936G>T ENSP00000513900.1:n.*1936G>T
ENST00000698734.1:c.*273G>T ENSP00000513901.1:n.*273G>T
ENST00000698735.1:n.2864G>T
ENST00000698736.1:n.2864G>T
ENST00000698737.1:n.2864G>T
ENST00000698738.1:n.2864G>T
ENST00000698739.1:n.2864G>T
ENST00000372371.8:c.2749G>T MANE Select ENSP00000361446.3:p.Glu917Ter
ENST00000372371.7:c.2749G>T ENSP00000361446.3:p.Glu917Ter
ENST00000472014.5:n.602G>T
NM_007055.3:c.2749G>T NP_008986.2:p.Glu917Ter
NM_007055.4:c.2749G>T MANE Select NP_008986.2:p.Glu917Ter