Canonical Allele Identifier: CA1921506567

Gene: POLR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000042_78000043delinsAT , CM000672.2:g.78000042_78000043delinsAT	GRCh38
NC_000010.10:g.79759800_79759801delinsAT , CM000672.1:g.79759800_79759801delinsAT	GRCh37
NC_000010.9:g.79429806_79429807delinsAT	NCBI36
NG_029648.1:g.34498_34499delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000698727.1:n.1614_1615delinsAT
ENST00000698728.1:n.2133_2134delinsAT
ENST00000698729.1:n.3679_3680delinsAT
ENST00000698730.1:n.3679_3680delinsAT
ENST00000698731.1:c.2413_2414delinsAT	ENSP00000513898.1:p.Met805=
ENST00000698732.1:c.*1415_*1416delinsAT	ENSP00000513899.1:n.*1415_*1416delinsAT
ENST00000698733.1:c.*1741_*1742delinsAT	ENSP00000513900.1:n.*1741_*1742delinsAT
ENST00000698734.1:c.2554_2555delinsAT	ENSP00000513901.1:p.Met852=
ENST00000698735.1:n.2669_2670delinsAT
ENST00000698736.1:n.2669_2670delinsAT
ENST00000698737.1:n.2669_2670delinsAT
ENST00000698738.1:n.2669_2670delinsAT
ENST00000698739.1:n.2669_2670delinsAT
ENST00000372371.8:c.2554_2555delinsAT MANE Select	ENSP00000361446.3:p.Met852=
ENST00000372371.7:c.2554_2555delinsAT	ENSP00000361446.3:p.Met852=
ENST00000472014.5:n.469+4673_469+4674delinsAT
NM_007055.3:c.2554_2555delinsAT	NP_008986.2:p.Met852=
NM_007055.4:c.2554_2555delinsAT MANE Select	NP_008986.2:p.Met852=