Canonical Allele Identifier: CA470397109

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759760T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000002T>A , CM000672.2:g.78000002T>A	GRCh38
NC_000010.10:g.79759760T>A , CM000672.1:g.79759760T>A	GRCh37
NC_000010.9:g.79429766T>A	NCBI36
NG_029648.1:g.34539A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1655A>T
ENST00000698728.1:n.2174A>T
ENST00000698729.1:n.3720A>T
ENST00000698730.1:n.3720A>T
ENST00000698731.1:c.2454A>T	ENSP00000513898.1:p.Thr818=
ENST00000698732.1:c.*1456A>T	ENSP00000513899.1:n.*1456A>T
ENST00000698733.1:c.*1782A>T	ENSP00000513900.1:n.*1782A>T
ENST00000698734.1:c.2595A>T	ENSP00000513901.1:p.Thr865=
ENST00000698735.1:n.2710A>T
ENST00000698736.1:n.2710A>T
ENST00000698737.1:n.2710A>T
ENST00000698738.1:n.2710A>T
ENST00000698739.1:n.2710A>T
ENST00000372371.8:c.2595A>T MANE Select	ENSP00000361446.3:p.Thr865=
ENST00000372371.7:c.2595A>T	ENSP00000361446.3:p.Thr865=
ENST00000472014.5:n.469+4714A>T
NM_007055.3:c.2595A>T	NP_008986.2:p.Thr865=
NM_007055.4:c.2595A>T MANE Select	NP_008986.2:p.Thr865=