Canonical Allele Identifier: CA377336996

Gene: POLR3A

Linked Data

• gnomAD v4: 10-78002235-C-T
• MyVariant Identifiers: chr10:g.79761993C>T (hg19) ; chr10:g.78002235C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78002235C>T , CM000672.2:g.78002235C>T	GRCh38
NC_000010.10:g.79761993C>T , CM000672.1:g.79761993C>T	GRCh37
NC_000010.9:g.79431999C>T	NCBI36
NG_029648.1:g.32306G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1381G>A
ENST00000698728.1:n.1900G>A
ENST00000698729.1:n.3446G>A
ENST00000698730.1:n.3446G>A
ENST00000698731.1:c.2180G>A	ENSP00000513898.1:p.Ser727Asn
ENST00000698732.1:c.*1182G>A	ENSP00000513899.1:n.*1182G>A
ENST00000698733.1:c.*1508G>A	ENSP00000513900.1:n.*1508G>A
ENST00000698734.1:c.2321G>A	ENSP00000513901.1:p.Ser774Asn
ENST00000698735.1:n.2436G>A
ENST00000698736.1:n.2436G>A
ENST00000698737.1:n.2436G>A
ENST00000698738.1:n.2436G>A
ENST00000698739.1:n.2436G>A
ENST00000372371.8:c.2321G>A MANE Select	ENSP00000361446.3:p.Ser774Asn
ENST00000372371.7:c.2321G>A	ENSP00000361446.3:p.Ser774Asn
ENST00000472014.5:n.469+2481G>A
ENST00000473588.2:c.984G>A
NM_007055.3:c.2321G>A	NP_008986.2:p.Ser774Asn
NM_007055.4:c.2321G>A MANE Select	NP_008986.2:p.Ser774Asn