Canonical Allele Identifier: CA377341061

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769699A>T (hg19) ; chr10:g.78009941A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009941A>T , CM000672.2:g.78009941A>T	GRCh38
NC_000010.10:g.79769699A>T , CM000672.1:g.79769699A>T	GRCh37
NC_000010.9:g.79439705A>T	NCBI36
NG_029648.1:g.24600T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698728.1:n.1272T>A
ENST00000698729.1:n.2818T>A
ENST00000698730.1:n.2818T>A
ENST00000698731.1:c.1552T>A	ENSP00000513898.1:p.Cys518Ser
ENST00000698732.1:c.*554T>A	ENSP00000513899.1:n.*554T>A
ENST00000698733.1:c.*880T>A	ENSP00000513900.1:n.*880T>A
ENST00000698734.1:c.1693T>A	ENSP00000513901.1:p.Cys565Ser
ENST00000698735.1:n.1808T>A
ENST00000698736.1:n.1808T>A
ENST00000698737.1:n.1808T>A
ENST00000698738.1:n.1808T>A
ENST00000698739.1:n.1808T>A
ENST00000372371.8:c.1693T>A MANE Select	ENSP00000361446.3:p.Cys565Ser
ENST00000372371.7:c.1693T>A	ENSP00000361446.3:p.Cys565Ser
ENST00000473588.2:c.495T>A
NM_007055.3:c.1693T>A	NP_008986.2:p.Cys565Ser
NM_007055.4:c.1693T>A MANE Select	NP_008986.2:p.Cys565Ser