Canonical Allele Identifier: CA470398299
Gene: POLR3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79769652T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78009894T>C , CM000672.2:g.78009894T>C GRCh38
NC_000010.10:g.79769652T>C , CM000672.1:g.79769652T>C GRCh37
NC_000010.9:g.79439658T>C NCBI36
NG_029648.1:g.24647A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698728.1:n.1319A>G
ENST00000698729.1:n.2865A>G
ENST00000698730.1:n.2865A>G
ENST00000698731.1:c.1599A>G ENSP00000513898.1:p.Lys533=
ENST00000698732.1:c.*601A>G ENSP00000513899.1:n.*601A>G
ENST00000698733.1:c.*927A>G ENSP00000513900.1:n.*927A>G
ENST00000698734.1:c.1740A>G ENSP00000513901.1:p.Lys580=
ENST00000698735.1:n.1855A>G
ENST00000698736.1:n.1855A>G
ENST00000698737.1:n.1855A>G
ENST00000698738.1:n.1855A>G
ENST00000698739.1:n.1855A>G
ENST00000372371.8:c.1740A>G MANE Select ENSP00000361446.3:p.Lys580=
ENST00000372371.7:c.1740A>G ENSP00000361446.3:p.Lys580=
ENST00000473588.2:c.542A>G
NM_007055.3:c.1740A>G NP_008986.2:p.Lys580=
NM_007055.4:c.1740A>G MANE Select NP_008986.2:p.Lys580=