Canonical Allele Identifier: CA377341177

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769737A>C (hg19) ; chr10:g.78009979A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009979A>C , CM000672.2:g.78009979A>C	GRCh38
NC_000010.10:g.79769737A>C , CM000672.1:g.79769737A>C	GRCh37
NC_000010.9:g.79439743A>C	NCBI36
NG_029648.1:g.24562T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698728.1:n.1234T>G
ENST00000698729.1:n.2780T>G
ENST00000698730.1:n.2780T>G
ENST00000698731.1:c.1514T>G	ENSP00000513898.1:p.Leu505Arg
ENST00000698732.1:c.*516T>G	ENSP00000513899.1:n.*516T>G
ENST00000698733.1:c.*842T>G	ENSP00000513900.1:n.*842T>G
ENST00000698734.1:c.1655T>G	ENSP00000513901.1:p.Leu552Arg
ENST00000698735.1:n.1770T>G
ENST00000698736.1:n.1770T>G
ENST00000698737.1:n.1770T>G
ENST00000698738.1:n.1770T>G
ENST00000698739.1:n.1770T>G
ENST00000372371.8:c.1655T>G MANE Select	ENSP00000361446.3:p.Leu552Arg
ENST00000372371.7:c.1655T>G	ENSP00000361446.3:p.Leu552Arg
ENST00000473588.2:c.457T>G
NM_007055.3:c.1655T>G	NP_008986.2:p.Leu552Arg
NM_007055.4:c.1655T>G MANE Select	NP_008986.2:p.Leu552Arg