Canonical Allele Identifier: CA377335414

Gene: POLR3A

Linked Data

• gnomAD v4: 10-77999987-G-T
• MyVariant Identifiers: chr10:g.79759745G>T (hg19) ; chr10:g.77999987G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77999987G>T , CM000672.2:g.77999987G>T	GRCh38
NC_000010.10:g.79759745G>T , CM000672.1:g.79759745G>T	GRCh37
NC_000010.9:g.79429751G>T	NCBI36
NG_029648.1:g.34554C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1670C>A
ENST00000698728.1:n.2189C>A
ENST00000698729.1:n.3735C>A
ENST00000698730.1:n.3735C>A
ENST00000698731.1:c.2469C>A	ENSP00000513898.1:p.Tyr823Ter
ENST00000698732.1:c.*1471C>A	ENSP00000513899.1:n.*1471C>A
ENST00000698733.1:c.*1797C>A	ENSP00000513900.1:n.*1797C>A
ENST00000698734.1:c.2610C>A	ENSP00000513901.1:p.Tyr870Ter
ENST00000698735.1:n.2725C>A
ENST00000698736.1:n.2725C>A
ENST00000698737.1:n.2725C>A
ENST00000698738.1:n.2725C>A
ENST00000698739.1:n.2725C>A
ENST00000372371.8:c.2610C>A MANE Select	ENSP00000361446.3:p.Tyr870Ter
ENST00000372371.7:c.2610C>A	ENSP00000361446.3:p.Tyr870Ter
ENST00000472014.5:n.469+4729C>A
NM_007055.3:c.2610C>A	NP_008986.2:p.Tyr870Ter
NM_007055.4:c.2610C>A MANE Select	NP_008986.2:p.Tyr870Ter