Canonical Allele Identifier: CA2609820172

Gene: POLR3A

Linked Data

• gnomAD v4: 10-77975822-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77975822G>T , CM000672.2:g.77975822G>T	GRCh38
NC_000010.10:g.79735580G>T , CM000672.1:g.79735580G>T	GRCh37
NC_000010.9:g.79405586G>T	NCBI36
NG_029648.1:g.58719C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.1941+4319C>A
ENST00000698725.1:n.3499C>A
ENST00000698726.1:n.5059C>A
ENST00000698727.1:n.4792C>A
ENST00000698728.1:n.5408C>A
ENST00000698729.1:n.6856C>A
ENST00000698730.1:n.6954C>A
ENST00000698731.1:c.*1656C>A	ENSP00000513898.1:n.*1656C>A
ENST00000698732.1:c.*4518C>A	ENSP00000513899.1:n.*4518C>A
ENST00000698733.1:c.*5016C>A	ENSP00000513900.1:n.*5016C>A
ENST00000698734.1:c.*4002C>A	ENSP00000513901.1:n.*4002C>A
ENST00000698735.1:n.6180C>A
ENST00000698736.1:n.6593C>A
ENST00000372371.8:c.*1656C>A MANE Select	ENSP00000361446.3:n.*1656C>A
ENST00000372371.7:c.*1656C>A	ENSP00000361446.3:n.*1656C>A
ENST00000616246.4:c.472+4319C>A	ENSP00000483738.1:n.472+4319C>A
NM_007055.3:c.*1656C>A	NP_008986.2:n.*1656C>A
NM_007055.4:c.*1656C>A MANE Select	NP_008986.2:n.*1656C>A