Canonical Allele Identifier: CA377326101

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739979A>G (hg19) ; chr10:g.77980221A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980221A>G , CM000672.2:g.77980221A>G	GRCh38
NC_000010.10:g.79739979A>G , CM000672.1:g.79739979A>G	GRCh37
NC_000010.9:g.79409985A>G	NCBI36
NG_029648.1:g.54320T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1861T>C
ENST00000698725.1:n.1614T>C
ENST00000698726.1:n.3174T>C
ENST00000698727.1:n.2907T>C
ENST00000698728.1:n.3523T>C
ENST00000698729.1:n.4971T>C
ENST00000698730.1:n.5069T>C
ENST00000698731.1:c.3803T>C	ENSP00000513898.1:p.Val1268Ala
ENST00000698732.1:c.*2633T>C	ENSP00000513899.1:n.*2633T>C
ENST00000698733.1:c.*3131T>C	ENSP00000513900.1:n.*3131T>C
ENST00000698734.1:c.*2117T>C	ENSP00000513901.1:n.*2117T>C
ENST00000698735.1:n.4295T>C
ENST00000698736.1:n.4708T>C
ENST00000698737.1:n.4059T>C
ENST00000372371.8:c.3944T>C MANE Select	ENSP00000361446.3:p.Val1315Ala
ENST00000372371.7:c.3944T>C	ENSP00000361446.3:p.Val1315Ala
ENST00000616246.4:c.392T>C	ENSP00000483738.1:p.Val131Ala
NM_007055.3:c.3944T>C	NP_008986.2:p.Val1315Ala
NM_007055.4:c.3944T>C MANE Select	NP_008986.2:p.Val1315Ala