Canonical Allele Identifier: CA470390625
Gene: POLR3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79739912C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980154C>T , CM000672.2:g.77980154C>T GRCh38
NC_000010.10:g.79739912C>T , CM000672.1:g.79739912C>T GRCh37
NC_000010.9:g.79409918C>T NCBI36
NG_029648.1:g.54387G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1928G>A
ENST00000698725.1:n.1681G>A
ENST00000698726.1:n.3241G>A
ENST00000698727.1:n.2974G>A
ENST00000698728.1:n.3590G>A
ENST00000698729.1:n.5038G>A
ENST00000698730.1:n.5136G>A
ENST00000698731.1:c.3870G>A ENSP00000513898.1:p.Lys1290=
ENST00000698732.1:c.*2700G>A ENSP00000513899.1:n.*2700G>A
ENST00000698733.1:c.*3198G>A ENSP00000513900.1:n.*3198G>A
ENST00000698734.1:c.*2184G>A ENSP00000513901.1:n.*2184G>A
ENST00000698735.1:n.4362G>A
ENST00000698736.1:n.4775G>A
ENST00000698737.1:n.4126G>A
ENST00000372371.8:c.4011G>A MANE Select ENSP00000361446.3:p.Lys1337=
ENST00000372371.7:c.4011G>A ENSP00000361446.3:p.Lys1337=
ENST00000616246.4:c.459G>A ENSP00000483738.1:p.Lys153=
NM_007055.3:c.4011G>A NP_008986.2:p.Lys1337=
NM_007055.4:c.4011G>A MANE Select NP_008986.2:p.Lys1337=