Canonical Allele Identifier: CA377340964

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769656A>C (hg19) ; chr10:g.78009898A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009898A>C , CM000672.2:g.78009898A>C	GRCh38
NC_000010.10:g.79769656A>C , CM000672.1:g.79769656A>C	GRCh37
NC_000010.9:g.79439662A>C	NCBI36
NG_029648.1:g.24643T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698728.1:n.1315T>G
ENST00000698729.1:n.2861T>G
ENST00000698730.1:n.2861T>G
ENST00000698731.1:c.1595T>G	ENSP00000513898.1:p.Ile532Ser
ENST00000698732.1:c.*597T>G	ENSP00000513899.1:n.*597T>G
ENST00000698733.1:c.*923T>G	ENSP00000513900.1:n.*923T>G
ENST00000698734.1:c.1736T>G	ENSP00000513901.1:p.Ile579Ser
ENST00000698735.1:n.1851T>G
ENST00000698736.1:n.1851T>G
ENST00000698737.1:n.1851T>G
ENST00000698738.1:n.1851T>G
ENST00000698739.1:n.1851T>G
ENST00000372371.8:c.1736T>G MANE Select	ENSP00000361446.3:p.Ile579Ser
ENST00000372371.7:c.1736T>G	ENSP00000361446.3:p.Ile579Ser
ENST00000473588.2:c.538T>G
NM_007055.3:c.1736T>G	NP_008986.2:p.Ile579Ser
NM_007055.4:c.1736T>G MANE Select	NP_008986.2:p.Ile579Ser