Canonical Allele Identifier: CA528011369

Gene: CDC73

Linked Data

• dbSNP Id: rs1558309875
• gnomAD v2: 1-193173224-CAT-C
• gnomAD v3: 1-193204094-CAT-C
• gnomAD v4: 1-193204094-CAT-C
• MyVariant Identifiers: chr1:g.193173226_193173228delinsA (hg19) ; chr1:g.193204096_193204098delinsA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193204096_193204097del , CM000663.2:g.193204096_193204097del	GRCh38
NC_000001.10:g.193173226_193173227del , CM000663.1:g.193173226_193173227del	GRCh37
NC_000001.9:g.191439849_191439850del	NCBI36
NG_012691.1:g.87139_87140del , LRG_507:g.87139_87140del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+244_1030+245del MANE Select	ENSP00000356405.4:n.1030+244_1030+245del
ENST00000635846.1:c.787+244_787+245del	ENSP00000490035.1:n.787+244_787+245del
ENST00000643006.1:c.1098+244_1098+245del	ENSP00000496633.1:n.1098+244_1098+245del
ENST00000648071.1:c.*1006+244_*1006+245del	ENSP00000497513.1:n.*1006+244_*1006+245del
ENST00000649613.1:n.280+244_280+245del
ENST00000649895.1:n.1248+244_1248+245del
ENST00000650197.1:c.1030+244_1030+245del	ENSP00000496929.1:n.1030+244_1030+245del
ENST00000367435.3:c.1030+244_1030+245del	ENSP00000356405.3:n.1030+244_1030+245del
NM_024529.4:c.1030+244_1030+245del , LRG_507t1:c.1030+244_1030+245del	NP_078805.3:n.1030+244_1030+245del
NM_024529.5:c.1030+244_1030+245del MANE Select	NP_078805.3:n.1030+244_1030+245del