Canonical Allele Identifier: CA470390669

Gene: POLR3A

Linked Data

• gnomAD v4: 10-77980229-C-T
• MyVariant Identifiers: chr10:g.79739987C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980229C>T , CM000672.2:g.77980229C>T	GRCh38
NC_000010.10:g.79739987C>T , CM000672.1:g.79739987C>T	GRCh37
NC_000010.9:g.79409993C>T	NCBI36
NG_029648.1:g.54312G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1853G>A
ENST00000698725.1:n.1606G>A
ENST00000698726.1:n.3166G>A
ENST00000698727.1:n.2899G>A
ENST00000698728.1:n.3515G>A
ENST00000698729.1:n.4963G>A
ENST00000698730.1:n.5061G>A
ENST00000698731.1:c.3795G>A	ENSP00000513898.1:p.Lys1265=
ENST00000698732.1:c.*2625G>A	ENSP00000513899.1:n.*2625G>A
ENST00000698733.1:c.*3123G>A	ENSP00000513900.1:n.*3123G>A
ENST00000698734.1:c.*2109G>A	ENSP00000513901.1:n.*2109G>A
ENST00000698735.1:n.4287G>A
ENST00000698736.1:n.4700G>A
ENST00000698737.1:n.4051G>A
ENST00000372371.8:c.3936G>A MANE Select	ENSP00000361446.3:p.Lys1312=
ENST00000372371.7:c.3936G>A	ENSP00000361446.3:p.Lys1312=
ENST00000616246.4:c.384G>A	ENSP00000483738.1:p.Lys128=
NM_007055.3:c.3936G>A	NP_008986.2:p.Lys1312=
NM_007055.4:c.3936G>A MANE Select	NP_008986.2:p.Lys1312=