Canonical Allele Identifier: CA377341215

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769746G>T (hg19) ; chr10:g.78009988G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009988G>T , CM000672.2:g.78009988G>T	GRCh38
NC_000010.10:g.79769746G>T , CM000672.1:g.79769746G>T	GRCh37
NC_000010.9:g.79439752G>T	NCBI36
NG_029648.1:g.24553C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698728.1:n.1225C>A
ENST00000698729.1:n.2771C>A
ENST00000698730.1:n.2771C>A
ENST00000698731.1:c.1505C>A	ENSP00000513898.1:p.Ala502Asp
ENST00000698732.1:c.*507C>A	ENSP00000513899.1:n.*507C>A
ENST00000698733.1:c.*833C>A	ENSP00000513900.1:n.*833C>A
ENST00000698734.1:c.1646C>A	ENSP00000513901.1:p.Ala549Asp
ENST00000698735.1:n.1761C>A
ENST00000698736.1:n.1761C>A
ENST00000698737.1:n.1761C>A
ENST00000698738.1:n.1761C>A
ENST00000698739.1:n.1761C>A
ENST00000372371.8:c.1646C>A MANE Select	ENSP00000361446.3:p.Ala549Asp
ENST00000372371.7:c.1646C>A	ENSP00000361446.3:p.Ala549Asp
ENST00000473588.2:c.448C>A
NM_007055.3:c.1646C>A	NP_008986.2:p.Ala549Asp
NM_007055.4:c.1646C>A MANE Select	NP_008986.2:p.Ala549Asp