Canonical Allele Identifier: CA377335539

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759805G>T (hg19) ; chr10:g.78000047G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000047G>T , CM000672.2:g.78000047G>T	GRCh38
NC_000010.10:g.79759805G>T , CM000672.1:g.79759805G>T	GRCh37
NC_000010.9:g.79429811G>T	NCBI36
NG_029648.1:g.34494C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698727.1:n.1610C>A
ENST00000698728.1:n.2129C>A
ENST00000698729.1:n.3675C>A
ENST00000698730.1:n.3675C>A
ENST00000698731.1:c.2409C>A	ENSP00000513898.1:p.His803Gln
ENST00000698732.1:c.*1411C>A	ENSP00000513899.1:n.*1411C>A
ENST00000698733.1:c.*1737C>A	ENSP00000513900.1:n.*1737C>A
ENST00000698734.1:c.2550C>A	ENSP00000513901.1:p.His850Gln
ENST00000698735.1:n.2665C>A
ENST00000698736.1:n.2665C>A
ENST00000698737.1:n.2665C>A
ENST00000698738.1:n.2665C>A
ENST00000698739.1:n.2665C>A
ENST00000372371.8:c.2550C>A MANE Select	ENSP00000361446.3:p.His850Gln
ENST00000372371.7:c.2550C>A	ENSP00000361446.3:p.His850Gln
ENST00000472014.5:n.469+4669C>A
NM_007055.3:c.2550C>A	NP_008986.2:p.His850Gln
NM_007055.4:c.2550C>A MANE Select	NP_008986.2:p.His850Gln