Canonical Allele Identifier: CA1010619073

Gene: CDC73

Linked Data

• dbSNP Id: rs1678049080
• gnomAD v3: 1-193251875-A-AAG
• gnomAD v4: 1-193251875-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251875_193251876insAG , CM000663.2:g.193251875_193251876insAG	GRCh38
NC_000001.10:g.193221005_193221006insAG , CM000663.1:g.193221005_193221006insAG	GRCh37
NC_000001.9:g.191487628_191487629insAG	NCBI36
NG_012691.1:g.134918_134919insAG , LRG_507:g.134918_134919insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*1163_*1164insAG MANE Select	ENSP00000356405.4:n.*1163_*1164insAG
ENST00000635846.1:c.*1163_*1164insAG	ENSP00000490035.1:n.*1163_*1164insAG
ENST00000643006.1:c.*1669_*1670insAG	ENSP00000496633.1:n.*1669_*1670insAG
ENST00000367435.3:c.*1163_*1164insAG	ENSP00000356405.3:n.*1163_*1164insAG
NM_024529.4:c.*1163_*1164insAG , LRG_507t1:c.*1163_*1164insAG	NP_078805.3:n.*1163_*1164insAG
NM_024529.5:c.*1163_*1164insAG MANE Select	NP_078805.3:n.*1163_*1164insAG