Canonical Allele Identifier: CA377340989

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79769666C>A (hg19) ; chr10:g.78009908C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009908C>A , CM000672.2:g.78009908C>A	GRCh38
NC_000010.10:g.79769666C>A , CM000672.1:g.79769666C>A	GRCh37
NC_000010.9:g.79439672C>A	NCBI36
NG_029648.1:g.24633G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698728.1:n.1305G>T
ENST00000698729.1:n.2851G>T
ENST00000698730.1:n.2851G>T
ENST00000698731.1:c.1585G>T	ENSP00000513898.1:p.Asp529Tyr
ENST00000698732.1:c.*587G>T	ENSP00000513899.1:n.*587G>T
ENST00000698733.1:c.*913G>T	ENSP00000513900.1:n.*913G>T
ENST00000698734.1:c.1726G>T	ENSP00000513901.1:p.Asp576Tyr
ENST00000698735.1:n.1841G>T
ENST00000698736.1:n.1841G>T
ENST00000698737.1:n.1841G>T
ENST00000698738.1:n.1841G>T
ENST00000698739.1:n.1841G>T
ENST00000372371.8:c.1726G>T MANE Select	ENSP00000361446.3:p.Asp576Tyr
ENST00000372371.7:c.1726G>T	ENSP00000361446.3:p.Asp576Tyr
ENST00000473588.2:c.528G>T
NM_007055.3:c.1726G>T	NP_008986.2:p.Asp576Tyr
NM_007055.4:c.1726G>T MANE Select	NP_008986.2:p.Asp576Tyr