Canonical Allele Identifier: CA343962685
Gene: CDC73 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193141987A>G , CM000663.2:g.193141987A>G GRCh38
NC_000001.10:g.193111117A>G , CM000663.1:g.193111117A>G GRCh37
NC_000001.9:g.191377740A>G NCBI36
NG_012691.1:g.25030A>G , LRG_507:g.25030A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.650A>G MANE Select ENSP00000356405.4:p.Glu217Gly
ENST00000635846.1:c.650A>G ENSP00000490035.1:p.Glu217Gly
ENST00000643006.1:c.650A>G ENSP00000496633.1:p.Glu217Gly
ENST00000643784.1:c.*126A>G ENSP00000494944.1:n.*126A>G
ENST00000647662.1:n.551A>G
ENST00000648071.1:c.*626A>G ENSP00000497513.1:n.*626A>G
ENST00000649606.1:n.663A>G
ENST00000649895.1:n.868A>G
ENST00000650197.1:c.650A>G ENSP00000496929.1:p.Glu217Gly
ENST00000367435.3:c.650A>G ENSP00000356405.3:p.Glu217Gly
NM_024529.4:c.650A>G , LRG_507t1:c.650A>G NP_078805.3:p.Glu217Gly
XM_006711537.2:c.650A>G XP_006711600.1:p.Glu217Gly
XM_006711537.4:c.650A>G XP_006711600.1:p.Glu217Gly
NM_024529.5:c.650A>G MANE Select NP_078805.3:p.Glu217Gly