Canonical Allele Identifier: CA470397610

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79764513C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78004755C>A , CM000672.2:g.78004755C>A	GRCh38
NC_000010.10:g.79764513C>A , CM000672.1:g.79764513C>A	GRCh37
NC_000010.9:g.79434519C>A	NCBI36
NG_029648.1:g.29786G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1268G>T
ENST00000698728.1:n.1787G>T
ENST00000698729.1:n.3333G>T
ENST00000698730.1:n.3333G>T
ENST00000698731.1:c.2067G>T	ENSP00000513898.1:p.Leu689=
ENST00000698732.1:c.*1069G>T	ENSP00000513899.1:n.*1069G>T
ENST00000698733.1:c.*1395G>T	ENSP00000513900.1:n.*1395G>T
ENST00000698734.1:c.2208G>T	ENSP00000513901.1:p.Leu736=
ENST00000698735.1:n.2323G>T
ENST00000698736.1:n.2323G>T
ENST00000698737.1:n.2323G>T
ENST00000698738.1:n.2323G>T
ENST00000698739.1:n.2323G>T
ENST00000372371.8:c.2208G>T MANE Select	ENSP00000361446.3:p.Leu736=
ENST00000372371.7:c.2208G>T	ENSP00000361446.3:p.Leu736=
ENST00000472014.5:n.430G>T
ENST00000473588.2:c.871G>T
NM_007055.3:c.2208G>T	NP_008986.2:p.Leu736=
NM_007055.4:c.2208G>T MANE Select	NP_008986.2:p.Leu736=