Canonical Allele Identifier: CA377341127

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769724G>T (hg19) ; chr10:g.78009966G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009966G>T , CM000672.2:g.78009966G>T	GRCh38
NC_000010.10:g.79769724G>T , CM000672.1:g.79769724G>T	GRCh37
NC_000010.9:g.79439730G>T	NCBI36
NG_029648.1:g.24575C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698728.1:n.1247C>A
ENST00000698729.1:n.2793C>A
ENST00000698730.1:n.2793C>A
ENST00000698731.1:c.1527C>A	ENSP00000513898.1:p.Asp509Glu
ENST00000698732.1:c.*529C>A	ENSP00000513899.1:n.*529C>A
ENST00000698733.1:c.*855C>A	ENSP00000513900.1:n.*855C>A
ENST00000698734.1:c.1668C>A	ENSP00000513901.1:p.Asp556Glu
ENST00000698735.1:n.1783C>A
ENST00000698736.1:n.1783C>A
ENST00000698737.1:n.1783C>A
ENST00000698738.1:n.1783C>A
ENST00000698739.1:n.1783C>A
ENST00000372371.8:c.1668C>A MANE Select	ENSP00000361446.3:p.Asp556Glu
ENST00000372371.7:c.1668C>A	ENSP00000361446.3:p.Asp556Glu
ENST00000473588.2:c.470C>A
NM_007055.3:c.1668C>A	NP_008986.2:p.Asp556Glu
NM_007055.4:c.1668C>A MANE Select	NP_008986.2:p.Asp556Glu