Canonical Allele Identifier: CA1303227

Gene: CDC73

Linked Data

• dbSNP Id: rs545666726
• ExAC: 1:193091319 A / AGG
• gnomAD v2: 1-193091319-A-AGG
• gnomAD v3: 1-193122189-A-AGG
• gnomAD v4: 1-193122189-A-AGG
• MyVariant Identifiers: chr1:g.193091320_193091321insGG (hg19) ; chr1:g.193091319_193091320insGG (hg19) ; chr1:g.193122190_193122191insGG (hg38) ; chr1:g.193122189_193122190insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122196_193122197dup , CM000663.2:g.193122196_193122197dup	GRCh38
NC_000001.10:g.193091326_193091327dup , CM000663.1:g.193091326_193091327dup	GRCh37
NC_000001.9:g.191357949_191357950dup	NCBI36
NG_012691.1:g.5239_5240dup , LRG_507:g.5239_5240dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-5_-4dup MANE Select	ENSP00000356405.4:n.-5_-4dup
ENST00000635846.1:c.-5_-4dup	ENSP00000490035.1:n.-5_-4dup
ENST00000643006.1:c.-5_-4dup	ENSP00000496633.1:n.-5_-4dup
ENST00000643784.1:c.-5_-4dup	ENSP00000494944.1:n.-5_-4dup
ENST00000648071.1:c.-5_-4dup	ENSP00000497513.1:n.-5_-4dup
ENST00000649606.1:n.9_10dup
ENST00000649895.1:n.214_215dup
ENST00000650197.1:c.-5_-4dup	ENSP00000496929.1:n.-5_-4dup
ENST00000367435.3:c.-5_-4dup	ENSP00000356405.3:n.-5_-4dup
NM_024529.4:c.-5_-4dup , LRG_507t1:c.-5_-4dup	NP_078805.3:n.-5_-4dup
XM_006711537.2:c.-5_-4dup	XP_006711600.1:n.-5_-4dup
XM_006711537.4:c.-5_-4dup	XP_006711600.1:n.-5_-4dup
XR_001738350.1:n.1466_1467dup
NM_024529.5:c.-5_-4dup MANE Select	NP_078805.3:n.-5_-4dup