Canonical Allele Identifier: CA377340930

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769636G>T (hg19) ; chr10:g.78009878G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009878G>T , CM000672.2:g.78009878G>T	GRCh38
NC_000010.10:g.79769636G>T , CM000672.1:g.79769636G>T	GRCh37
NC_000010.9:g.79439642G>T	NCBI36
NG_029648.1:g.24663C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698728.1:n.1335C>A
ENST00000698729.1:n.2881C>A
ENST00000698730.1:n.2881C>A
ENST00000698731.1:c.1615C>A	ENSP00000513898.1:p.Pro539Thr
ENST00000698732.1:c.*617C>A	ENSP00000513899.1:n.*617C>A
ENST00000698733.1:c.*943C>A	ENSP00000513900.1:n.*943C>A
ENST00000698734.1:c.1756C>A	ENSP00000513901.1:p.Pro586Thr
ENST00000698735.1:n.1871C>A
ENST00000698736.1:n.1871C>A
ENST00000698737.1:n.1871C>A
ENST00000698738.1:n.1871C>A
ENST00000698739.1:n.1871C>A
ENST00000372371.8:c.1756C>A MANE Select	ENSP00000361446.3:p.Pro586Thr
ENST00000372371.7:c.1756C>A	ENSP00000361446.3:p.Pro586Thr
ENST00000473588.2:c.558C>A
NM_007055.3:c.1756C>A	NP_008986.2:p.Pro586Thr
NM_007055.4:c.1756C>A MANE Select	NP_008986.2:p.Pro586Thr