Canonical Allele Identifier: CA377326014

Gene: POLR3A

Linked Data

• gnomAD v4: 10-77980182-A-G
• MyVariant Identifiers: chr10:g.79739940A>G (hg19) ; chr10:g.77980182A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980182A>G , CM000672.2:g.77980182A>G	GRCh38
NC_000010.10:g.79739940A>G , CM000672.1:g.79739940A>G	GRCh37
NC_000010.9:g.79409946A>G	NCBI36
NG_029648.1:g.54359T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1900T>C
ENST00000698725.1:n.1653T>C
ENST00000698726.1:n.3213T>C
ENST00000698727.1:n.2946T>C
ENST00000698728.1:n.3562T>C
ENST00000698729.1:n.5010T>C
ENST00000698730.1:n.5108T>C
ENST00000698731.1:c.3842T>C	ENSP00000513898.1:p.Leu1281Pro
ENST00000698732.1:c.*2672T>C	ENSP00000513899.1:n.*2672T>C
ENST00000698733.1:c.*3170T>C	ENSP00000513900.1:n.*3170T>C
ENST00000698734.1:c.*2156T>C	ENSP00000513901.1:n.*2156T>C
ENST00000698735.1:n.4334T>C
ENST00000698736.1:n.4747T>C
ENST00000698737.1:n.4098T>C
ENST00000372371.8:c.3983T>C MANE Select	ENSP00000361446.3:p.Leu1328Pro
ENST00000372371.7:c.3983T>C	ENSP00000361446.3:p.Leu1328Pro
ENST00000616246.4:c.431T>C	ENSP00000483738.1:p.Leu144Pro
NM_007055.3:c.3983T>C	NP_008986.2:p.Leu1328Pro
NM_007055.4:c.3983T>C MANE Select	NP_008986.2:p.Leu1328Pro