Canonical Allele Identifier: CA377341018

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769680A>G (hg19) ; chr10:g.78009922A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009922A>G , CM000672.2:g.78009922A>G	GRCh38
NC_000010.10:g.79769680A>G , CM000672.1:g.79769680A>G	GRCh37
NC_000010.9:g.79439686A>G	NCBI36
NG_029648.1:g.24619T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698728.1:n.1291T>C
ENST00000698729.1:n.2837T>C
ENST00000698730.1:n.2837T>C
ENST00000698731.1:c.1571T>C	ENSP00000513898.1:p.Ile524Thr
ENST00000698732.1:c.*573T>C	ENSP00000513899.1:n.*573T>C
ENST00000698733.1:c.*899T>C	ENSP00000513900.1:n.*899T>C
ENST00000698734.1:c.1712T>C	ENSP00000513901.1:p.Ile571Thr
ENST00000698735.1:n.1827T>C
ENST00000698736.1:n.1827T>C
ENST00000698737.1:n.1827T>C
ENST00000698738.1:n.1827T>C
ENST00000698739.1:n.1827T>C
ENST00000372371.8:c.1712T>C MANE Select	ENSP00000361446.3:p.Ile571Thr
ENST00000372371.7:c.1712T>C	ENSP00000361446.3:p.Ile571Thr
ENST00000473588.2:c.514T>C
NM_007055.3:c.1712T>C	NP_008986.2:p.Ile571Thr
NM_007055.4:c.1712T>C MANE Select	NP_008986.2:p.Ile571Thr