Canonical Allele Identifier: CA2609820181

Gene: POLR3A

Linked Data

• gnomAD v4: 10-77975833-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77975833G>T , CM000672.2:g.77975833G>T	GRCh38
NC_000010.10:g.79735591G>T , CM000672.1:g.79735591G>T	GRCh37
NC_000010.9:g.79405597G>T	NCBI36
NG_029648.1:g.58708C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.1941+4308C>A
ENST00000698725.1:n.3488C>A
ENST00000698726.1:n.5048C>A
ENST00000698727.1:n.4781C>A
ENST00000698728.1:n.5397C>A
ENST00000698729.1:n.6845C>A
ENST00000698730.1:n.6943C>A
ENST00000698731.1:c.*1645C>A	ENSP00000513898.1:n.*1645C>A
ENST00000698732.1:c.*4507C>A	ENSP00000513899.1:n.*4507C>A
ENST00000698733.1:c.*5005C>A	ENSP00000513900.1:n.*5005C>A
ENST00000698734.1:c.*3991C>A	ENSP00000513901.1:n.*3991C>A
ENST00000698735.1:n.6169C>A
ENST00000698736.1:n.6582C>A
ENST00000372371.8:c.*1645C>A MANE Select	ENSP00000361446.3:n.*1645C>A
ENST00000372371.7:c.*1645C>A	ENSP00000361446.3:n.*1645C>A
ENST00000616246.4:c.472+4308C>A	ENSP00000483738.1:n.472+4308C>A
NM_007055.3:c.*1645C>A	NP_008986.2:n.*1645C>A
NM_007055.4:c.*1645C>A MANE Select	NP_008986.2:n.*1645C>A