Canonical Allele Identifier: CA470397129

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759778G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000020G>C , CM000672.2:g.78000020G>C	GRCh38
NC_000010.10:g.79759778G>C , CM000672.1:g.79759778G>C	GRCh37
NC_000010.9:g.79429784G>C	NCBI36
NG_029648.1:g.34521C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1637C>G
ENST00000698728.1:n.2156C>G
ENST00000698729.1:n.3702C>G
ENST00000698730.1:n.3702C>G
ENST00000698731.1:c.2436C>G	ENSP00000513898.1:p.Val812=
ENST00000698732.1:c.*1438C>G	ENSP00000513899.1:n.*1438C>G
ENST00000698733.1:c.*1764C>G	ENSP00000513900.1:n.*1764C>G
ENST00000698734.1:c.2577C>G	ENSP00000513901.1:p.Val859=
ENST00000698735.1:n.2692C>G
ENST00000698736.1:n.2692C>G
ENST00000698737.1:n.2692C>G
ENST00000698738.1:n.2692C>G
ENST00000698739.1:n.2692C>G
ENST00000372371.8:c.2577C>G MANE Select	ENSP00000361446.3:p.Val859=
ENST00000372371.7:c.2577C>G	ENSP00000361446.3:p.Val859=
ENST00000472014.5:n.469+4696C>G
NM_007055.3:c.2577C>G	NP_008986.2:p.Val859=
NM_007055.4:c.2577C>G MANE Select	NP_008986.2:p.Val859=