Canonical Allele Identifier: CA2609820242

Gene: POLR3A

Linked Data

• gnomAD v4: 10-77975933-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77975933A>G , CM000672.2:g.77975933A>G	GRCh38
NC_000010.10:g.79735691A>G , CM000672.1:g.79735691A>G	GRCh37
NC_000010.9:g.79405697A>G	NCBI36
NG_029648.1:g.58608T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.1941+4208T>C
ENST00000698725.1:n.3388T>C
ENST00000698726.1:n.4948T>C
ENST00000698727.1:n.4681T>C
ENST00000698728.1:n.5297T>C
ENST00000698729.1:n.6745T>C
ENST00000698730.1:n.6843T>C
ENST00000698731.1:c.*1545T>C	ENSP00000513898.1:n.*1545T>C
ENST00000698732.1:c.*4407T>C	ENSP00000513899.1:n.*4407T>C
ENST00000698733.1:c.*4905T>C	ENSP00000513900.1:n.*4905T>C
ENST00000698734.1:c.*3891T>C	ENSP00000513901.1:n.*3891T>C
ENST00000698735.1:n.6069T>C
ENST00000698736.1:n.6482T>C
ENST00000372371.8:c.*1545T>C MANE Select	ENSP00000361446.3:n.*1545T>C
ENST00000372371.7:c.*1545T>C	ENSP00000361446.3:n.*1545T>C
ENST00000616246.4:c.472+4208T>C	ENSP00000483738.1:n.472+4208T>C
NM_007055.3:c.*1545T>C	NP_008986.2:n.*1545T>C
NM_007055.4:c.*1545T>C MANE Select	NP_008986.2:n.*1545T>C