Canonical Allele Identifier: CA377333880

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79752965T>G (hg19) ; chr10:g.77993207T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77993207T>G , CM000672.2:g.77993207T>G	GRCh38
NC_000010.10:g.79752965T>G , CM000672.1:g.79752965T>G	GRCh37
NC_000010.9:g.79422971T>G	NCBI36
NG_029648.1:g.41334A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.45A>C
ENST00000698727.1:n.1837A>C
ENST00000698728.1:n.2356A>C
ENST00000698729.1:n.3902A>C
ENST00000698730.1:n.3902A>C
ENST00000698731.1:c.2636A>C	ENSP00000513898.1:p.Asp879Ala
ENST00000698732.1:c.*1638A>C	ENSP00000513899.1:n.*1638A>C
ENST00000698733.1:c.*1964A>C	ENSP00000513900.1:n.*1964A>C
ENST00000698734.1:c.*301A>C	ENSP00000513901.1:n.*301A>C
ENST00000698735.1:n.2892A>C
ENST00000698736.1:n.2892A>C
ENST00000698737.1:n.2892A>C
ENST00000698738.1:n.2892A>C
ENST00000698739.1:n.2892A>C
ENST00000372371.8:c.2777A>C MANE Select	ENSP00000361446.3:p.Asp926Ala
ENST00000372371.7:c.2777A>C	ENSP00000361446.3:p.Asp926Ala
ENST00000472014.5:n.630A>C
NM_007055.3:c.2777A>C	NP_008986.2:p.Asp926Ala
NM_007055.4:c.2777A>C MANE Select	NP_008986.2:p.Asp926Ala