Canonical Allele Identifier: CA377335553

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759810A>T (hg19) ; chr10:g.78000052A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000052A>T , CM000672.2:g.78000052A>T	GRCh38
NC_000010.10:g.79759810A>T , CM000672.1:g.79759810A>T	GRCh37
NC_000010.9:g.79429816A>T	NCBI36
NG_029648.1:g.34489T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1605T>A
ENST00000698728.1:n.2124T>A
ENST00000698729.1:n.3670T>A
ENST00000698730.1:n.3670T>A
ENST00000698731.1:c.2404T>A	ENSP00000513898.1:p.Phe802Ile
ENST00000698732.1:c.*1406T>A	ENSP00000513899.1:n.*1406T>A
ENST00000698733.1:c.*1732T>A	ENSP00000513900.1:n.*1732T>A
ENST00000698734.1:c.2545T>A	ENSP00000513901.1:p.Phe849Ile
ENST00000698735.1:n.2660T>A
ENST00000698736.1:n.2660T>A
ENST00000698737.1:n.2660T>A
ENST00000698738.1:n.2660T>A
ENST00000698739.1:n.2660T>A
ENST00000372371.8:c.2545T>A MANE Select	ENSP00000361446.3:p.Phe849Ile
ENST00000372371.7:c.2545T>A	ENSP00000361446.3:p.Phe849Ile
ENST00000472014.5:n.469+4664T>A
NM_007055.3:c.2545T>A	NP_008986.2:p.Phe849Ile
NM_007055.4:c.2545T>A MANE Select	NP_008986.2:p.Phe849Ile