Canonical Allele Identifier: CA377335728
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78000091T>C , CM000672.2:g.78000091T>C GRCh38
NC_000010.10:g.79759849T>C , CM000672.1:g.79759849T>C GRCh37
NC_000010.9:g.79429855T>C NCBI36
NG_029648.1:g.34450A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698727.1:n.1566A>G
ENST00000698728.1:n.2085A>G
ENST00000698729.1:n.3631A>G
ENST00000698730.1:n.3631A>G
ENST00000698731.1:c.2365A>G ENSP00000513898.1:p.Asn789Asp
ENST00000698732.1:c.*1367A>G ENSP00000513899.1:n.*1367A>G
ENST00000698733.1:c.*1693A>G ENSP00000513900.1:n.*1693A>G
ENST00000698734.1:c.2506A>G ENSP00000513901.1:p.Asn836Asp
ENST00000698735.1:n.2621A>G
ENST00000698736.1:n.2621A>G
ENST00000698737.1:n.2621A>G
ENST00000698738.1:n.2621A>G
ENST00000698739.1:n.2621A>G
ENST00000372371.8:c.2506A>G MANE Select ENSP00000361446.3:p.Asn836Asp
ENST00000372371.7:c.2506A>G ENSP00000361446.3:p.Asn836Asp
ENST00000472014.5:n.469+4625A>G
NM_007055.3:c.2506A>G NP_008986.2:p.Asn836Asp
NM_007055.4:c.2506A>G MANE Select NP_008986.2:p.Asn836Asp