Canonical Allele Identifier: CA2574591319

Gene: POLR3A

Linked Data

• gnomAD v4: 10-77980314-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980314A>G , CM000672.2:g.77980314A>G	GRCh38
NC_000010.10:g.79740072A>G , CM000672.1:g.79740072A>G	GRCh37
NC_000010.9:g.79410078A>G	NCBI36
NG_029648.1:g.54227T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1809-41T>C
ENST00000698725.1:n.1521T>C
ENST00000698726.1:n.3122-41T>C
ENST00000698727.1:n.2855-41T>C
ENST00000698728.1:n.3471-41T>C
ENST00000698729.1:n.4919-41T>C
ENST00000698730.1:n.5017-41T>C
ENST00000698731.1:c.3751-41T>C	ENSP00000513898.1:n.3751-41T>C
ENST00000698732.1:c.*2581-41T>C	ENSP00000513899.1:n.*2581-41T>C
ENST00000698733.1:c.*3079-41T>C	ENSP00000513900.1:n.*3079-41T>C
ENST00000698734.1:c.*2065-41T>C	ENSP00000513901.1:n.*2065-41T>C
ENST00000698735.1:n.4243-41T>C
ENST00000698736.1:n.4656-41T>C
ENST00000698737.1:n.4007-41T>C
ENST00000372371.8:c.3892-41T>C MANE Select	ENSP00000361446.3:n.3892-41T>C
ENST00000372371.7:c.3892-41T>C	ENSP00000361446.3:n.3892-41T>C
ENST00000616246.4:c.340-41T>C	ENSP00000483738.1:n.340-41T>C
NM_007055.3:c.3892-41T>C	NP_008986.2:n.3892-41T>C
NM_007055.4:c.3892-41T>C MANE Select	NP_008986.2:n.3892-41T>C