Canonical Allele Identifier: CA35098868

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193212105G>A , CM000663.2:g.193212105G>A	GRCh38
NC_000001.10:g.193181235G>A , CM000663.1:g.193181235G>A	GRCh37
NC_000001.9:g.191447858G>A	NCBI36
NG_012691.1:g.95148G>A , LRG_507:g.95148G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.1066+5G>A MANE Select	NP_078805.3:n.1066+5G>A
ENST00000367435.5:c.1066+5G>A MANE Select	ENSP00000356405.4:n.1066+5G>A
NM_024529.4:c.1066+5G>A , LRG_507t1:c.1066+5G>A	NP_078805.3:n.1066+5G>A
ENST00000367435.3:c.1066+5G>A	ENSP00000356405.3:n.1066+5G>A
ENST00000635846.1:c.823+5G>A	ENSP00000490035.1:n.823+5G>A
ENST00000643006.1:c.1134+5G>A	ENSP00000496633.1:n.1134+5G>A
ENST00000648071.1:c.*1042+5G>A	ENSP00000497513.1:n.*1042+5G>A
ENST00000649613.1:n.316+5G>A
ENST00000649895.1:n.1284+5G>A
ENST00000650197.1:c.1066+5G>A	ENSP00000496929.1:n.1066+5G>A