Canonical Allele Identifier: CA377326235

Gene: POLR3A

Linked Data

• gnomAD v4: 10-77980273-C-T
• MyVariant Identifiers: chr10:g.79740031C>T (hg19) ; chr10:g.77980273C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980273C>T , CM000672.2:g.77980273C>T	GRCh38
NC_000010.10:g.79740031C>T , CM000672.1:g.79740031C>T	GRCh37
NC_000010.9:g.79410037C>T	NCBI36
NG_029648.1:g.54268G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1809G>A
ENST00000698725.1:n.1562G>A
ENST00000698726.1:n.3122G>A
ENST00000698727.1:n.2855G>A
ENST00000698728.1:n.3471G>A
ENST00000698729.1:n.4919G>A
ENST00000698730.1:n.5017G>A
ENST00000698731.1:c.3751G>A	ENSP00000513898.1:p.Gly1251Ser
ENST00000698732.1:c.*2581G>A	ENSP00000513899.1:n.*2581G>A
ENST00000698733.1:c.*3079G>A	ENSP00000513900.1:n.*3079G>A
ENST00000698734.1:c.*2065G>A	ENSP00000513901.1:n.*2065G>A
ENST00000698735.1:n.4243G>A
ENST00000698736.1:n.4656G>A
ENST00000698737.1:n.4007G>A
ENST00000372371.8:c.3892G>A MANE Select	ENSP00000361446.3:p.Gly1298Ser
ENST00000372371.7:c.3892G>A	ENSP00000361446.3:p.Gly1298Ser
ENST00000616246.4:c.340G>A	ENSP00000483738.1:p.Gly114Ser
NM_007055.3:c.3892G>A	NP_008986.2:p.Gly1298Ser
NM_007055.4:c.3892G>A MANE Select	NP_008986.2:p.Gly1298Ser