Canonical Allele Identifier: CA377326103

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739980C>A (hg19) ; chr10:g.77980222C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980222C>A , CM000672.2:g.77980222C>A	GRCh38
NC_000010.10:g.79739980C>A , CM000672.1:g.79739980C>A	GRCh37
NC_000010.9:g.79409986C>A	NCBI36
NG_029648.1:g.54319G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1860G>T
ENST00000698725.1:n.1613G>T
ENST00000698726.1:n.3173G>T
ENST00000698727.1:n.2906G>T
ENST00000698728.1:n.3522G>T
ENST00000698729.1:n.4970G>T
ENST00000698730.1:n.5068G>T
ENST00000698731.1:c.3802G>T	ENSP00000513898.1:p.Val1268Leu
ENST00000698732.1:c.*2632G>T	ENSP00000513899.1:n.*2632G>T
ENST00000698733.1:c.*3130G>T	ENSP00000513900.1:n.*3130G>T
ENST00000698734.1:c.*2116G>T	ENSP00000513901.1:n.*2116G>T
ENST00000698735.1:n.4294G>T
ENST00000698736.1:n.4707G>T
ENST00000698737.1:n.4058G>T
ENST00000372371.8:c.3943G>T MANE Select	ENSP00000361446.3:p.Val1315Leu
ENST00000372371.7:c.3943G>T	ENSP00000361446.3:p.Val1315Leu
ENST00000616246.4:c.391G>T	ENSP00000483738.1:p.Val131Leu
NM_007055.3:c.3943G>T	NP_008986.2:p.Val1315Leu
NM_007055.4:c.3943G>T MANE Select	NP_008986.2:p.Val1315Leu