Canonical Allele Identifier: CA377325949

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739911C>G (hg19) ; chr10:g.77980153C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980153C>G , CM000672.2:g.77980153C>G	GRCh38
NC_000010.10:g.79739911C>G , CM000672.1:g.79739911C>G	GRCh37
NC_000010.9:g.79409917C>G	NCBI36
NG_029648.1:g.54388G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1929G>C
ENST00000698725.1:n.1682G>C
ENST00000698726.1:n.3242G>C
ENST00000698727.1:n.2975G>C
ENST00000698728.1:n.3591G>C
ENST00000698729.1:n.5039G>C
ENST00000698730.1:n.5137G>C
ENST00000698731.1:c.3871G>C	ENSP00000513898.1:p.Asp1291His
ENST00000698732.1:c.*2701G>C	ENSP00000513899.1:n.*2701G>C
ENST00000698733.1:c.*3199G>C	ENSP00000513900.1:n.*3199G>C
ENST00000698734.1:c.*2185G>C	ENSP00000513901.1:n.*2185G>C
ENST00000698735.1:n.4363G>C
ENST00000698736.1:n.4776G>C
ENST00000698737.1:n.4127G>C
ENST00000372371.8:c.4012G>C MANE Select	ENSP00000361446.3:p.Asp1338His
ENST00000372371.7:c.4012G>C	ENSP00000361446.3:p.Asp1338His
ENST00000616246.4:c.460G>C	ENSP00000483738.1:p.Asp154His
NM_007055.3:c.4012G>C	NP_008986.2:p.Asp1338His
NM_007055.4:c.4012G>C MANE Select	NP_008986.2:p.Asp1338His