Canonical Allele Identifier: CA377326135

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739992T>C (hg19) ; chr10:g.77980234T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980234T>C , CM000672.2:g.77980234T>C	GRCh38
NC_000010.10:g.79739992T>C , CM000672.1:g.79739992T>C	GRCh37
NC_000010.9:g.79409998T>C	NCBI36
NG_029648.1:g.54307A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1848A>G
ENST00000698725.1:n.1601A>G
ENST00000698726.1:n.3161A>G
ENST00000698727.1:n.2894A>G
ENST00000698728.1:n.3510A>G
ENST00000698729.1:n.4958A>G
ENST00000698730.1:n.5056A>G
ENST00000698731.1:c.3790A>G	ENSP00000513898.1:p.Met1264Val
ENST00000698732.1:c.*2620A>G	ENSP00000513899.1:n.*2620A>G
ENST00000698733.1:c.*3118A>G	ENSP00000513900.1:n.*3118A>G
ENST00000698734.1:c.*2104A>G	ENSP00000513901.1:n.*2104A>G
ENST00000698735.1:n.4282A>G
ENST00000698736.1:n.4695A>G
ENST00000698737.1:n.4046A>G
ENST00000372371.8:c.3931A>G MANE Select	ENSP00000361446.3:p.Met1311Val
ENST00000372371.7:c.3931A>G	ENSP00000361446.3:p.Met1311Val
ENST00000616246.4:c.379A>G	ENSP00000483738.1:p.Met127Val
NM_007055.3:c.3931A>G	NP_008986.2:p.Met1311Val
NM_007055.4:c.3931A>G MANE Select	NP_008986.2:p.Met1311Val