Canonical Allele Identifier: CA470390659

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739969C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980211C>G , CM000672.2:g.77980211C>G	GRCh38
NC_000010.10:g.79739969C>G , CM000672.1:g.79739969C>G	GRCh37
NC_000010.9:g.79409975C>G	NCBI36
NG_029648.1:g.54330G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1871G>C
ENST00000698725.1:n.1624G>C
ENST00000698726.1:n.3184G>C
ENST00000698727.1:n.2917G>C
ENST00000698728.1:n.3533G>C
ENST00000698729.1:n.4981G>C
ENST00000698730.1:n.5079G>C
ENST00000698731.1:c.3813G>C	ENSP00000513898.1:p.Leu1271=
ENST00000698732.1:c.*2643G>C	ENSP00000513899.1:n.*2643G>C
ENST00000698733.1:c.*3141G>C	ENSP00000513900.1:n.*3141G>C
ENST00000698734.1:c.*2127G>C	ENSP00000513901.1:n.*2127G>C
ENST00000698735.1:n.4305G>C
ENST00000698736.1:n.4718G>C
ENST00000698737.1:n.4069G>C
ENST00000372371.8:c.3954G>C MANE Select	ENSP00000361446.3:p.Leu1318=
ENST00000372371.7:c.3954G>C	ENSP00000361446.3:p.Leu1318=
ENST00000616246.4:c.402G>C	ENSP00000483738.1:p.Leu134=
NM_007055.3:c.3954G>C	NP_008986.2:p.Leu1318=
NM_007055.4:c.3954G>C MANE Select	NP_008986.2:p.Leu1318=