Canonical Allele Identifier: CA377341113

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769720A>T (hg19) ; chr10:g.78009962A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009962A>T , CM000672.2:g.78009962A>T	GRCh38
NC_000010.10:g.79769720A>T , CM000672.1:g.79769720A>T	GRCh37
NC_000010.9:g.79439726A>T	NCBI36
NG_029648.1:g.24579T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698728.1:n.1251T>A
ENST00000698729.1:n.2797T>A
ENST00000698730.1:n.2797T>A
ENST00000698731.1:c.1531T>A	ENSP00000513898.1:p.Phe511Ile
ENST00000698732.1:c.*533T>A	ENSP00000513899.1:n.*533T>A
ENST00000698733.1:c.*859T>A	ENSP00000513900.1:n.*859T>A
ENST00000698734.1:c.1672T>A	ENSP00000513901.1:p.Phe558Ile
ENST00000698735.1:n.1787T>A
ENST00000698736.1:n.1787T>A
ENST00000698737.1:n.1787T>A
ENST00000698738.1:n.1787T>A
ENST00000698739.1:n.1787T>A
ENST00000372371.8:c.1672T>A MANE Select	ENSP00000361446.3:p.Phe558Ile
ENST00000372371.7:c.1672T>A	ENSP00000361446.3:p.Phe558Ile
ENST00000473588.2:c.474T>A
NM_007055.3:c.1672T>A	NP_008986.2:p.Phe558Ile
NM_007055.4:c.1672T>A MANE Select	NP_008986.2:p.Phe558Ile