Canonical Allele Identifier: CA470390649

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739951C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980193C>A , CM000672.2:g.77980193C>A	GRCh38
NC_000010.10:g.79739951C>A , CM000672.1:g.79739951C>A	GRCh37
NC_000010.9:g.79409957C>A	NCBI36
NG_029648.1:g.54348G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1889G>T
ENST00000698725.1:n.1642G>T
ENST00000698726.1:n.3202G>T
ENST00000698727.1:n.2935G>T
ENST00000698728.1:n.3551G>T
ENST00000698729.1:n.4999G>T
ENST00000698730.1:n.5097G>T
ENST00000698731.1:c.3831G>T	ENSP00000513898.1:p.Thr1277=
ENST00000698732.1:c.*2661G>T	ENSP00000513899.1:n.*2661G>T
ENST00000698733.1:c.*3159G>T	ENSP00000513900.1:n.*3159G>T
ENST00000698734.1:c.*2145G>T	ENSP00000513901.1:n.*2145G>T
ENST00000698735.1:n.4323G>T
ENST00000698736.1:n.4736G>T
ENST00000698737.1:n.4087G>T
ENST00000372371.8:c.3972G>T MANE Select	ENSP00000361446.3:p.Thr1324=
ENST00000372371.7:c.3972G>T	ENSP00000361446.3:p.Thr1324=
ENST00000616246.4:c.420G>T	ENSP00000483738.1:p.Thr140=
NM_007055.3:c.3972G>T	NP_008986.2:p.Thr1324=
NM_007055.4:c.3972G>T MANE Select	NP_008986.2:p.Thr1324=