Canonical Allele Identifier: CA377326155

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79740001G>C (hg19) ; chr10:g.77980243G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980243G>C , CM000672.2:g.77980243G>C	GRCh38
NC_000010.10:g.79740001G>C , CM000672.1:g.79740001G>C	GRCh37
NC_000010.9:g.79410007G>C	NCBI36
NG_029648.1:g.54298C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1839C>G
ENST00000698725.1:n.1592C>G
ENST00000698726.1:n.3152C>G
ENST00000698727.1:n.2885C>G
ENST00000698728.1:n.3501C>G
ENST00000698729.1:n.4949C>G
ENST00000698730.1:n.5047C>G
ENST00000698731.1:c.3781C>G	ENSP00000513898.1:p.Leu1261Val
ENST00000698732.1:c.*2611C>G	ENSP00000513899.1:n.*2611C>G
ENST00000698733.1:c.*3109C>G	ENSP00000513900.1:n.*3109C>G
ENST00000698734.1:c.*2095C>G	ENSP00000513901.1:n.*2095C>G
ENST00000698735.1:n.4273C>G
ENST00000698736.1:n.4686C>G
ENST00000698737.1:n.4037C>G
ENST00000372371.8:c.3922C>G MANE Select	ENSP00000361446.3:p.Leu1308Val
ENST00000372371.7:c.3922C>G	ENSP00000361446.3:p.Leu1308Val
ENST00000616246.4:c.370C>G	ENSP00000483738.1:p.Leu124Val
NM_007055.3:c.3922C>G	NP_008986.2:p.Leu1308Val
NM_007055.4:c.3922C>G MANE Select	NP_008986.2:p.Leu1308Val