Canonical Allele Identifier: CA377341030

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769687C>A (hg19) ; chr10:g.78009929C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009929C>A , CM000672.2:g.78009929C>A	GRCh38
NC_000010.10:g.79769687C>A , CM000672.1:g.79769687C>A	GRCh37
NC_000010.9:g.79439693C>A	NCBI36
NG_029648.1:g.24612G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698728.1:n.1284G>T
ENST00000698729.1:n.2830G>T
ENST00000698730.1:n.2830G>T
ENST00000698731.1:c.1564G>T	ENSP00000513898.1:p.Ala522Ser
ENST00000698732.1:c.*566G>T	ENSP00000513899.1:n.*566G>T
ENST00000698733.1:c.*892G>T	ENSP00000513900.1:n.*892G>T
ENST00000698734.1:c.1705G>T	ENSP00000513901.1:p.Ala569Ser
ENST00000698735.1:n.1820G>T
ENST00000698736.1:n.1820G>T
ENST00000698737.1:n.1820G>T
ENST00000698738.1:n.1820G>T
ENST00000698739.1:n.1820G>T
ENST00000372371.8:c.1705G>T MANE Select	ENSP00000361446.3:p.Ala569Ser
ENST00000372371.7:c.1705G>T	ENSP00000361446.3:p.Ala569Ser
ENST00000473588.2:c.507G>T
NM_007055.3:c.1705G>T	NP_008986.2:p.Ala569Ser
NM_007055.4:c.1705G>T MANE Select	NP_008986.2:p.Ala569Ser