Canonical Allele Identifier: CA2528648749

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203971_193203972insT , CM000663.2:g.193203971_193203972insT	GRCh38
NC_000001.10:g.193173101_193173102insT , CM000663.1:g.193173101_193173102insT	GRCh37
NC_000001.9:g.191439724_191439725insT	NCBI36
NG_012691.1:g.87014_87015insT , LRG_507:g.87014_87015insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+119_1030+120insT MANE Select	ENSP00000356405.4:n.1030+119_1030+120insT
ENST00000635846.1:c.787+119_787+120insT	ENSP00000490035.1:n.787+119_787+120insT
ENST00000643006.1:c.1098+119_1098+120insT	ENSP00000496633.1:n.1098+119_1098+120insT
ENST00000648071.1:c.*1006+119_*1006+120insT	ENSP00000497513.1:n.*1006+119_*1006+120insT
ENST00000649613.1:n.280+119_280+120insT
ENST00000649895.1:n.1248+119_1248+120insT
ENST00000650197.1:c.1030+119_1030+120insT	ENSP00000496929.1:n.1030+119_1030+120insT
ENST00000367435.3:c.1030+119_1030+120insT	ENSP00000356405.3:n.1030+119_1030+120insT
NM_024529.4:c.1030+119_1030+120insT , LRG_507t1:c.1030+119_1030+120insT	NP_078805.3:n.1030+119_1030+120insT
NM_024529.5:c.1030+119_1030+120insT MANE Select	NP_078805.3:n.1030+119_1030+120insT