Canonical Allele Identifier: CA377326016

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739941G>T (hg19) ; chr10:g.77980183G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980183G>T , CM000672.2:g.77980183G>T	GRCh38
NC_000010.10:g.79739941G>T , CM000672.1:g.79739941G>T	GRCh37
NC_000010.9:g.79409947G>T	NCBI36
NG_029648.1:g.54358C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1899C>A
ENST00000698725.1:n.1652C>A
ENST00000698726.1:n.3212C>A
ENST00000698727.1:n.2945C>A
ENST00000698728.1:n.3561C>A
ENST00000698729.1:n.5009C>A
ENST00000698730.1:n.5107C>A
ENST00000698731.1:c.3841C>A	ENSP00000513898.1:p.Leu1281Ile
ENST00000698732.1:c.*2671C>A	ENSP00000513899.1:n.*2671C>A
ENST00000698733.1:c.*3169C>A	ENSP00000513900.1:n.*3169C>A
ENST00000698734.1:c.*2155C>A	ENSP00000513901.1:n.*2155C>A
ENST00000698735.1:n.4333C>A
ENST00000698736.1:n.4746C>A
ENST00000698737.1:n.4097C>A
ENST00000372371.8:c.3982C>A MANE Select	ENSP00000361446.3:p.Leu1328Ile
ENST00000372371.7:c.3982C>A	ENSP00000361446.3:p.Leu1328Ile
ENST00000616246.4:c.430C>A	ENSP00000483738.1:p.Leu144Ile
NM_007055.3:c.3982C>A	NP_008986.2:p.Leu1328Ile
NM_007055.4:c.3982C>A MANE Select	NP_008986.2:p.Leu1328Ile