Canonical Allele Identifier: CA377334065

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79753001C>A (hg19) ; chr10:g.77993243C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77993243C>A , CM000672.2:g.77993243C>A	GRCh38
NC_000010.10:g.79753001C>A , CM000672.1:g.79753001C>A	GRCh37
NC_000010.9:g.79423007C>A	NCBI36
NG_029648.1:g.41298G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.9G>T
ENST00000698727.1:n.1801G>T
ENST00000698728.1:n.2320G>T
ENST00000698729.1:n.3866G>T
ENST00000698730.1:n.3866G>T
ENST00000698731.1:c.2600G>T	ENSP00000513898.1:p.Gly867Val
ENST00000698732.1:c.*1602G>T	ENSP00000513899.1:n.*1602G>T
ENST00000698733.1:c.*1928G>T	ENSP00000513900.1:n.*1928G>T
ENST00000698734.1:c.*265G>T	ENSP00000513901.1:n.*265G>T
ENST00000698735.1:n.2856G>T
ENST00000698736.1:n.2856G>T
ENST00000698737.1:n.2856G>T
ENST00000698738.1:n.2856G>T
ENST00000698739.1:n.2856G>T
ENST00000372371.8:c.2741G>T MANE Select	ENSP00000361446.3:p.Gly914Val
ENST00000372371.7:c.2741G>T	ENSP00000361446.3:p.Gly914Val
ENST00000472014.5:n.594G>T
NM_007055.3:c.2741G>T	NP_008986.2:p.Gly914Val
NM_007055.4:c.2741G>T MANE Select	NP_008986.2:p.Gly914Val