Canonical Allele Identifier: CA343962817
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs2103126478

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193142048C>G , CM000663.2:g.193142048C>G GRCh38
NC_000001.10:g.193111178C>G , CM000663.1:g.193111178C>G GRCh37
NC_000001.9:g.191377801C>G NCBI36
NG_012691.1:g.25091C>G , LRG_507:g.25091C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.711C>G MANE Select ENSP00000356405.4:p.Ile237Met
ENST00000635846.1:c.711C>G ENSP00000490035.1:p.Ile237Met
ENST00000643006.1:c.711C>G ENSP00000496633.1:p.Ile237Met
ENST00000643784.1:c.*187C>G ENSP00000494944.1:n.*187C>G
ENST00000647662.1:n.612C>G
ENST00000648071.1:c.*687C>G ENSP00000497513.1:n.*687C>G
ENST00000649606.1:n.724C>G
ENST00000649895.1:n.929C>G
ENST00000650197.1:c.711C>G ENSP00000496929.1:p.Ile237Met
ENST00000367435.3:c.711C>G ENSP00000356405.3:p.Ile237Met
NM_024529.4:c.711C>G , LRG_507t1:c.711C>G NP_078805.3:p.Ile237Met
XM_006711537.2:c.711C>G XP_006711600.1:p.Ile237Met
XM_006711537.4:c.711C>G XP_006711600.1:p.Ile237Met
NM_024529.5:c.711C>G MANE Select NP_078805.3:p.Ile237Met