Canonical Allele Identifier: CA377326162
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980247A>C , CM000672.2:g.77980247A>C GRCh38
NC_000010.10:g.79740005A>C , CM000672.1:g.79740005A>C GRCh37
NC_000010.9:g.79410011A>C NCBI36
NG_029648.1:g.54294T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1835T>G
ENST00000698725.1:n.1588T>G
ENST00000698726.1:n.3148T>G
ENST00000698727.1:n.2881T>G
ENST00000698728.1:n.3497T>G
ENST00000698729.1:n.4945T>G
ENST00000698730.1:n.5043T>G
ENST00000698731.1:c.3777T>G ENSP00000513898.1:p.Phe1259Leu
ENST00000698732.1:c.*2607T>G ENSP00000513899.1:n.*2607T>G
ENST00000698733.1:c.*3105T>G ENSP00000513900.1:n.*3105T>G
ENST00000698734.1:c.*2091T>G ENSP00000513901.1:n.*2091T>G
ENST00000698735.1:n.4269T>G
ENST00000698736.1:n.4682T>G
ENST00000698737.1:n.4033T>G
ENST00000372371.8:c.3918T>G MANE Select ENSP00000361446.3:p.Phe1306Leu
ENST00000372371.7:c.3918T>G ENSP00000361446.3:p.Phe1306Leu
ENST00000616246.4:c.366T>G ENSP00000483738.1:p.Phe122Leu
NM_007055.3:c.3918T>G NP_008986.2:p.Phe1306Leu
NM_007055.4:c.3918T>G MANE Select NP_008986.2:p.Phe1306Leu