Canonical Allele Identifier: CA2649631005
Gene: CDC73 HGNC NCBI

Linked Data

gnomAD v4: 1-193251425-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251425A>G , CM000663.2:g.193251425A>G GRCh38
NC_000001.10:g.193220555A>G , CM000663.1:g.193220555A>G GRCh37
NC_000001.9:g.191487178A>G NCBI36
NG_012691.1:g.134468A>G , LRG_507:g.134468A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*713A>G MANE Select ENSP00000356405.4:n.*713A>G
ENST00000635846.1:c.*713A>G ENSP00000490035.1:n.*713A>G
ENST00000643006.1:c.*1219A>G ENSP00000496633.1:n.*1219A>G
ENST00000367435.3:c.*713A>G ENSP00000356405.3:n.*713A>G
NM_024529.4:c.*713A>G , LRG_507t1:c.*713A>G NP_078805.3:n.*713A>G
NM_024529.5:c.*713A>G MANE Select NP_078805.3:n.*713A>G
Search 100 bp 5'
Search 100 bp 3'