Canonical Allele Identifier: CA1216150010

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203922_193203925delinsTATA , CM000663.2:g.193203922_193203925delinsTATA	GRCh38
NC_000001.10:g.193173052_193173055delinsTATA , CM000663.1:g.193173052_193173055delinsTATA	GRCh37
NC_000001.9:g.191439675_191439678delinsTATA	NCBI36
NG_012691.1:g.86965_86968delinsTATA , LRG_507:g.86965_86968delinsTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+70_1030+73delinsTATA MANE Select	ENSP00000356405.4:n.1030+70_1030+73delinsTATA
ENST00000635846.1:c.787+70_787+73delinsTATA	ENSP00000490035.1:n.787+70_787+73delinsTATA
ENST00000643006.1:c.1098+70_1098+73delinsTATA	ENSP00000496633.1:n.1098+70_1098+73delinsTATA
ENST00000648071.1:c.*1006+70_*1006+73delinsTATA	ENSP00000497513.1:n.*1006+70_*1006+73delinsTATA
ENST00000649613.1:n.280+70_280+73delinsTATA
ENST00000649895.1:n.1248+70_1248+73delinsTATA
ENST00000650197.1:c.1030+70_1030+73delinsTATA	ENSP00000496929.1:n.1030+70_1030+73delinsTATA
ENST00000367435.3:c.1030+70_1030+73delinsTATA	ENSP00000356405.3:n.1030+70_1030+73delinsTATA
NM_024529.4:c.1030+70_1030+73delinsTATA , LRG_507t1:c.1030+70_1030+73delinsTATA	NP_078805.3:n.1030+70_1030+73delinsTATA
NM_024529.5:c.1030+70_1030+73delinsTATA MANE Select	NP_078805.3:n.1030+70_1030+73delinsTATA