Canonical Allele Identifier: CA377326114

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739984C>A (hg19) ; chr10:g.77980226C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980226C>A , CM000672.2:g.77980226C>A	GRCh38
NC_000010.10:g.79739984C>A , CM000672.1:g.79739984C>A	GRCh37
NC_000010.9:g.79409990C>A	NCBI36
NG_029648.1:g.54315G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1856G>T
ENST00000698725.1:n.1609G>T
ENST00000698726.1:n.3169G>T
ENST00000698727.1:n.2902G>T
ENST00000698728.1:n.3518G>T
ENST00000698729.1:n.4966G>T
ENST00000698730.1:n.5064G>T
ENST00000698731.1:c.3798G>T	ENSP00000513898.1:p.Glu1266Asp
ENST00000698732.1:c.*2628G>T	ENSP00000513899.1:n.*2628G>T
ENST00000698733.1:c.*3126G>T	ENSP00000513900.1:n.*3126G>T
ENST00000698734.1:c.*2112G>T	ENSP00000513901.1:n.*2112G>T
ENST00000698735.1:n.4290G>T
ENST00000698736.1:n.4703G>T
ENST00000698737.1:n.4054G>T
ENST00000372371.8:c.3939G>T MANE Select	ENSP00000361446.3:p.Glu1313Asp
ENST00000372371.7:c.3939G>T	ENSP00000361446.3:p.Glu1313Asp
ENST00000616246.4:c.387G>T	ENSP00000483738.1:p.Glu129Asp
NM_007055.3:c.3939G>T	NP_008986.2:p.Glu1313Asp
NM_007055.4:c.3939G>T MANE Select	NP_008986.2:p.Glu1313Asp