Canonical Allele Identifier: CA210182899

Gene: POLR3A

Linked Data

• dbSNP Id: rs972897855
• MyVariant Identifiers: chr10:g.79735586del (hg19) ; chr10:g.77975828del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77975828del , CM000672.2:g.77975828del	GRCh38
NC_000010.10:g.79735586del , CM000672.1:g.79735586del	GRCh37
NC_000010.9:g.79405592del	NCBI36
NG_029648.1:g.58713del

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.1941+4313del
ENST00000698725.1:n.3493del
ENST00000698726.1:n.5053del
ENST00000698727.1:n.4786del
ENST00000698728.1:n.5402del
ENST00000698729.1:n.6850del
ENST00000698730.1:n.6948del
ENST00000698731.1:c.*1650del	ENSP00000513898.1:n.*1650del
ENST00000698732.1:c.*4512del	ENSP00000513899.1:n.*4512del
ENST00000698733.1:c.*5010del	ENSP00000513900.1:n.*5010del
ENST00000698734.1:c.*3996del	ENSP00000513901.1:n.*3996del
ENST00000698735.1:n.6174del
ENST00000698736.1:n.6587del
ENST00000372371.8:c.*1650del MANE Select	ENSP00000361446.3:n.*1650del
ENST00000372371.7:c.*1650del	ENSP00000361446.3:n.*1650del
ENST00000616246.4:c.472+4313del	ENSP00000483738.1:n.472+4313del
NM_007055.3:c.*1650del	NP_008986.2:n.*1650del
NM_007055.4:c.*1650del MANE Select	NP_008986.2:n.*1650del