Canonical Allele Identifier: CA377326018

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739942A>C (hg19) ; chr10:g.77980184A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980184A>C , CM000672.2:g.77980184A>C	GRCh38
NC_000010.10:g.79739942A>C , CM000672.1:g.79739942A>C	GRCh37
NC_000010.9:g.79409948A>C	NCBI36
NG_029648.1:g.54357T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1898T>G
ENST00000698725.1:n.1651T>G
ENST00000698726.1:n.3211T>G
ENST00000698727.1:n.2944T>G
ENST00000698728.1:n.3560T>G
ENST00000698729.1:n.5008T>G
ENST00000698730.1:n.5106T>G
ENST00000698731.1:c.3840T>G	ENSP00000513898.1:p.His1280Gln
ENST00000698732.1:c.*2670T>G	ENSP00000513899.1:n.*2670T>G
ENST00000698733.1:c.*3168T>G	ENSP00000513900.1:n.*3168T>G
ENST00000698734.1:c.*2154T>G	ENSP00000513901.1:n.*2154T>G
ENST00000698735.1:n.4332T>G
ENST00000698736.1:n.4745T>G
ENST00000698737.1:n.4096T>G
ENST00000372371.8:c.3981T>G MANE Select	ENSP00000361446.3:p.His1327Gln
ENST00000372371.7:c.3981T>G	ENSP00000361446.3:p.His1327Gln
ENST00000616246.4:c.429T>G	ENSP00000483738.1:p.His143Gln
NM_007055.3:c.3981T>G	NP_008986.2:p.His1327Gln
NM_007055.4:c.3981T>G MANE Select	NP_008986.2:p.His1327Gln