Canonical Allele Identifier: CA377340998

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769671C>T (hg19) ; chr10:g.78009913C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009913C>T , CM000672.2:g.78009913C>T	GRCh38
NC_000010.10:g.79769671C>T , CM000672.1:g.79769671C>T	GRCh37
NC_000010.9:g.79439677C>T	NCBI36
NG_029648.1:g.24628G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698728.1:n.1300G>A
ENST00000698729.1:n.2846G>A
ENST00000698730.1:n.2846G>A
ENST00000698731.1:c.1580G>A	ENSP00000513898.1:p.Gly527Asp
ENST00000698732.1:c.*582G>A	ENSP00000513899.1:n.*582G>A
ENST00000698733.1:c.*908G>A	ENSP00000513900.1:n.*908G>A
ENST00000698734.1:c.1721G>A	ENSP00000513901.1:p.Gly574Asp
ENST00000698735.1:n.1836G>A
ENST00000698736.1:n.1836G>A
ENST00000698737.1:n.1836G>A
ENST00000698738.1:n.1836G>A
ENST00000698739.1:n.1836G>A
ENST00000372371.8:c.1721G>A MANE Select	ENSP00000361446.3:p.Gly574Asp
ENST00000372371.7:c.1721G>A	ENSP00000361446.3:p.Gly574Asp
ENST00000473588.2:c.523G>A
NM_007055.3:c.1721G>A	NP_008986.2:p.Gly574Asp
NM_007055.4:c.1721G>A MANE Select	NP_008986.2:p.Gly574Asp