Canonical Allele Identifier: CA729323277
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1285538569
gnomAD v3: 1-193251935-A-AT
gnomAD v4: 1-193251935-A-AT
MyVariant Identifiers: chr1:g.193221065_193221066insT (hg19) chr1:g.193251935_193251936insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251942dup , CM000663.2:g.193251942dup GRCh38
NC_000001.10:g.193221072dup , CM000663.1:g.193221072dup GRCh37
NC_000001.9:g.191487695dup NCBI36
NG_012691.1:g.134985dup , LRG_507:g.134985dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1230dup MANE Select ENSP00000356405.4:n.*1230dup
ENST00000635846.1:c.*1230dup ENSP00000490035.1:n.*1230dup
ENST00000643006.1:c.*1736dup ENSP00000496633.1:n.*1736dup
ENST00000367435.3:c.*1230dup ENSP00000356405.3:n.*1230dup
NM_024529.4:c.*1230dup , LRG_507t1:c.*1230dup NP_078805.3:n.*1230dup
NM_024529.5:c.*1230dup MANE Select NP_078805.3:n.*1230dup
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