Canonical Allele Identifier: CA528019102
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1228924908
gnomAD v2: 1-193220765-TCC-T
gnomAD v3: 1-193251635-TCC-T
gnomAD v4: 1-193251635-TCC-T
MyVariant Identifiers: chr1:g.193220766_193220767del (hg19) chr1:g.193251636_193251637del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251637_193251638del , CM000663.2:g.193251637_193251638del GRCh38
NC_000001.10:g.193220767_193220768del , CM000663.1:g.193220767_193220768del GRCh37
NC_000001.9:g.191487390_191487391del NCBI36
NG_012691.1:g.134680_134681del , LRG_507:g.134680_134681del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*925_*926del MANE Select ENSP00000356405.4:n.*925_*926del
ENST00000635846.1:c.*925_*926del ENSP00000490035.1:n.*925_*926del
ENST00000643006.1:c.*1431_*1432del ENSP00000496633.1:n.*1431_*1432del
ENST00000367435.3:c.*925_*926del ENSP00000356405.3:n.*925_*926del
NM_024529.4:c.*925_*926del , LRG_507t1:c.*925_*926del NP_078805.3:n.*925_*926del
NM_024529.5:c.*925_*926del MANE Select NP_078805.3:n.*925_*926del
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