Canonical Allele Identifier: CA377326064

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739961A>G (hg19) ; chr10:g.77980203A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980203A>G , CM000672.2:g.77980203A>G	GRCh38
NC_000010.10:g.79739961A>G , CM000672.1:g.79739961A>G	GRCh37
NC_000010.9:g.79409967A>G	NCBI36
NG_029648.1:g.54338T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1879T>C
ENST00000698725.1:n.1632T>C
ENST00000698726.1:n.3192T>C
ENST00000698727.1:n.2925T>C
ENST00000698728.1:n.3541T>C
ENST00000698729.1:n.4989T>C
ENST00000698730.1:n.5087T>C
ENST00000698731.1:c.3821T>C	ENSP00000513898.1:p.Phe1274Ser
ENST00000698732.1:c.*2651T>C	ENSP00000513899.1:n.*2651T>C
ENST00000698733.1:c.*3149T>C	ENSP00000513900.1:n.*3149T>C
ENST00000698734.1:c.*2135T>C	ENSP00000513901.1:n.*2135T>C
ENST00000698735.1:n.4313T>C
ENST00000698736.1:n.4726T>C
ENST00000698737.1:n.4077T>C
ENST00000372371.8:c.3962T>C MANE Select	ENSP00000361446.3:p.Phe1321Ser
ENST00000372371.7:c.3962T>C	ENSP00000361446.3:p.Phe1321Ser
ENST00000616246.4:c.410T>C	ENSP00000483738.1:p.Phe137Ser
NM_007055.3:c.3962T>C	NP_008986.2:p.Phe1321Ser
NM_007055.4:c.3962T>C MANE Select	NP_008986.2:p.Phe1321Ser