Canonical Allele Identifier: CA1010608179
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1675460456
gnomAD v3: 1-193122169-GC-G
gnomAD v4: 1-193122169-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122173del , CM000663.2:g.193122173del GRCh38
NC_000001.10:g.193091303del , CM000663.1:g.193091303del GRCh37
NC_000001.9:g.191357926del NCBI36
NG_012691.1:g.5216del , LRG_507:g.5216del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-28del MANE Select ENSP00000356405.4:n.-28del
ENST00000643006.1:c.-28del ENSP00000496633.1:n.-28del
ENST00000643784.1:c.-28del ENSP00000494944.1:n.-28del
ENST00000649895.1:n.191del
ENST00000650197.1:c.-28del ENSP00000496929.1:n.-28del
ENST00000367435.3:c.-28del ENSP00000356405.3:n.-28del
NM_024529.4:c.-28del , LRG_507t1:c.-28del NP_078805.3:n.-28del
XM_006711537.2:c.-28del XP_006711600.1:n.-28del
XM_006711537.4:c.-28del XP_006711600.1:n.-28del
XR_001738350.1:n.1487del
NM_024529.5:c.-28del MANE Select NP_078805.3:n.-28del
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