Canonical Allele Identifier: CA2609820238

Gene: POLR3A

Linked Data

• gnomAD v4: 10-77975914-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77975914G>T , CM000672.2:g.77975914G>T	GRCh38
NC_000010.10:g.79735672G>T , CM000672.1:g.79735672G>T	GRCh37
NC_000010.9:g.79405678G>T	NCBI36
NG_029648.1:g.58627C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.1941+4227C>A
ENST00000698725.1:n.3407C>A
ENST00000698726.1:n.4967C>A
ENST00000698727.1:n.4700C>A
ENST00000698728.1:n.5316C>A
ENST00000698729.1:n.6764C>A
ENST00000698730.1:n.6862C>A
ENST00000698731.1:c.*1564C>A	ENSP00000513898.1:n.*1564C>A
ENST00000698732.1:c.*4426C>A	ENSP00000513899.1:n.*4426C>A
ENST00000698733.1:c.*4924C>A	ENSP00000513900.1:n.*4924C>A
ENST00000698734.1:c.*3910C>A	ENSP00000513901.1:n.*3910C>A
ENST00000698735.1:n.6088C>A
ENST00000698736.1:n.6501C>A
ENST00000372371.8:c.*1564C>A MANE Select	ENSP00000361446.3:n.*1564C>A
ENST00000372371.7:c.*1564C>A	ENSP00000361446.3:n.*1564C>A
ENST00000616246.4:c.472+4227C>A	ENSP00000483738.1:n.472+4227C>A
NM_007055.3:c.*1564C>A	NP_008986.2:n.*1564C>A
NM_007055.4:c.*1564C>A MANE Select	NP_008986.2:n.*1564C>A