Canonical Allele Identifier: CA470397119

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759769A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000011A>C , CM000672.2:g.78000011A>C	GRCh38
NC_000010.10:g.79759769A>C , CM000672.1:g.79759769A>C	GRCh37
NC_000010.9:g.79429775A>C	NCBI36
NG_029648.1:g.34530T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1646T>G
ENST00000698728.1:n.2165T>G
ENST00000698729.1:n.3711T>G
ENST00000698730.1:n.3711T>G
ENST00000698731.1:c.2445T>G	ENSP00000513898.1:p.Ala815=
ENST00000698732.1:c.*1447T>G	ENSP00000513899.1:n.*1447T>G
ENST00000698733.1:c.*1773T>G	ENSP00000513900.1:n.*1773T>G
ENST00000698734.1:c.2586T>G	ENSP00000513901.1:p.Ala862=
ENST00000698735.1:n.2701T>G
ENST00000698736.1:n.2701T>G
ENST00000698737.1:n.2701T>G
ENST00000698738.1:n.2701T>G
ENST00000698739.1:n.2701T>G
ENST00000372371.8:c.2586T>G MANE Select	ENSP00000361446.3:p.Ala862=
ENST00000372371.7:c.2586T>G	ENSP00000361446.3:p.Ala862=
ENST00000472014.5:n.469+4705T>G
NM_007055.3:c.2586T>G	NP_008986.2:p.Ala862=
NM_007055.4:c.2586T>G MANE Select	NP_008986.2:p.Ala862=