Canonical Allele Identifier: CA35103598
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs998973442
gnomAD v2: 1-193220970-C-A
gnomAD v3: 1-193251840-C-A
gnomAD v4: 1-193251840-C-A
MyVariant Identifiers: chr1:g.193220970C>A (hg19) chr1:g.193220970_193220974delinsATTTG (hg19) chr1:g.193251840C>A (hg38) chr1:g.193251840_193251844delinsATTTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251840C>A , CM000663.2:g.193251840C>A GRCh38
NC_000001.10:g.193220970C>A , CM000663.1:g.193220970C>A GRCh37
NC_000001.9:g.191487593C>A NCBI36
NG_012691.1:g.134883C>A , LRG_507:g.134883C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1128C>A MANE Select ENSP00000356405.4:n.*1128C>A
ENST00000635846.1:c.*1128C>A ENSP00000490035.1:n.*1128C>A
ENST00000643006.1:c.*1634C>A ENSP00000496633.1:n.*1634C>A
ENST00000367435.3:c.*1128C>A ENSP00000356405.3:n.*1128C>A
NM_024529.4:c.*1128C>A , LRG_507t1:c.*1128C>A NP_078805.3:n.*1128C>A
NM_024529.5:c.*1128C>A MANE Select NP_078805.3:n.*1128C>A
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