Canonical Allele Identifier: CA1216150079

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193204113_193204114delinsTA , CM000663.2:g.193204113_193204114delinsTA	GRCh38
NC_000001.10:g.193173243_193173244delinsTA , CM000663.1:g.193173243_193173244delinsTA	GRCh37
NC_000001.9:g.191439866_191439867delinsTA	NCBI36
NG_012691.1:g.87156_87157delinsTA , LRG_507:g.87156_87157delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+261_1030+262delinsTA MANE Select	ENSP00000356405.4:n.1030+261_1030+262delinsTA
ENST00000635846.1:c.787+261_787+262delinsTA	ENSP00000490035.1:n.787+261_787+262delinsTA
ENST00000643006.1:c.1098+261_1098+262delinsTA	ENSP00000496633.1:n.1098+261_1098+262delinsTA
ENST00000648071.1:c.*1006+261_*1006+262delinsTA	ENSP00000497513.1:n.*1006+261_*1006+262delinsTA
ENST00000649613.1:n.280+261_280+262delinsTA
ENST00000649895.1:n.1248+261_1248+262delinsTA
ENST00000650197.1:c.1030+261_1030+262delinsTA	ENSP00000496929.1:n.1030+261_1030+262delinsTA
ENST00000367435.3:c.1030+261_1030+262delinsTA	ENSP00000356405.3:n.1030+261_1030+262delinsTA
NM_024529.4:c.1030+261_1030+262delinsTA , LRG_507t1:c.1030+261_1030+262delinsTA	NP_078805.3:n.1030+261_1030+262delinsTA
NM_024529.5:c.1030+261_1030+262delinsTA MANE Select	NP_078805.3:n.1030+261_1030+262delinsTA