Canonical Allele Identifier: CA377326021

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739943T>C (hg19) ; chr10:g.77980185T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980185T>C , CM000672.2:g.77980185T>C	GRCh38
NC_000010.10:g.79739943T>C , CM000672.1:g.79739943T>C	GRCh37
NC_000010.9:g.79409949T>C	NCBI36
NG_029648.1:g.54356A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1897A>G
ENST00000698725.1:n.1650A>G
ENST00000698726.1:n.3210A>G
ENST00000698727.1:n.2943A>G
ENST00000698728.1:n.3559A>G
ENST00000698729.1:n.5007A>G
ENST00000698730.1:n.5105A>G
ENST00000698731.1:c.3839A>G	ENSP00000513898.1:p.His1280Arg
ENST00000698732.1:c.*2669A>G	ENSP00000513899.1:n.*2669A>G
ENST00000698733.1:c.*3167A>G	ENSP00000513900.1:n.*3167A>G
ENST00000698734.1:c.*2153A>G	ENSP00000513901.1:n.*2153A>G
ENST00000698735.1:n.4331A>G
ENST00000698736.1:n.4744A>G
ENST00000698737.1:n.4095A>G
ENST00000372371.8:c.3980A>G MANE Select	ENSP00000361446.3:p.His1327Arg
ENST00000372371.7:c.3980A>G	ENSP00000361446.3:p.His1327Arg
ENST00000616246.4:c.428A>G	ENSP00000483738.1:p.His143Arg
NM_007055.3:c.3980A>G	NP_008986.2:p.His1327Arg
NM_007055.4:c.3980A>G MANE Select	NP_008986.2:p.His1327Arg