Canonical Allele Identifier: CA470397130
Gene: POLR3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79759781T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78000023T>A , CM000672.2:g.78000023T>A GRCh38
NC_000010.10:g.79759781T>A , CM000672.1:g.79759781T>A GRCh37
NC_000010.9:g.79429787T>A NCBI36
NG_029648.1:g.34518A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698727.1:n.1634A>T
ENST00000698728.1:n.2153A>T
ENST00000698729.1:n.3699A>T
ENST00000698730.1:n.3699A>T
ENST00000698731.1:c.2433A>T ENSP00000513898.1:p.Leu811=
ENST00000698732.1:c.*1435A>T ENSP00000513899.1:n.*1435A>T
ENST00000698733.1:c.*1761A>T ENSP00000513900.1:n.*1761A>T
ENST00000698734.1:c.2574A>T ENSP00000513901.1:p.Leu858=
ENST00000698735.1:n.2689A>T
ENST00000698736.1:n.2689A>T
ENST00000698737.1:n.2689A>T
ENST00000698738.1:n.2689A>T
ENST00000698739.1:n.2689A>T
ENST00000372371.8:c.2574A>T MANE Select ENSP00000361446.3:p.Leu858=
ENST00000372371.7:c.2574A>T ENSP00000361446.3:p.Leu858=
ENST00000472014.5:n.469+4693A>T
NM_007055.3:c.2574A>T NP_008986.2:p.Leu858=
NM_007055.4:c.2574A>T MANE Select NP_008986.2:p.Leu858=