Canonical Allele Identifier: CA344078571

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193218962A>G (hg19) ; chr1:g.193249832A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193249832A>G , CM000663.2:g.193249832A>G	GRCh38
NC_000001.10:g.193218962A>G , CM000663.1:g.193218962A>G	GRCh37
NC_000001.9:g.191485585A>G	NCBI36
NG_012691.1:g.132875A>G , LRG_507:g.132875A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1520A>G MANE Select	ENSP00000356405.4:p.Asp507Gly
ENST00000635846.1:c.1277A>G	ENSP00000490035.1:p.Asp426Gly
ENST00000643006.1:c.*430A>G	ENSP00000496633.1:n.*430A>G
ENST00000648071.1:c.*1496A>G	ENSP00000497513.1:n.*1496A>G
ENST00000649613.1:n.770A>G
ENST00000650197.1:c.*218A>G	ENSP00000496929.1:n.*218A>G
ENST00000367435.3:c.1520A>G	ENSP00000356405.3:p.Asp507Gly
ENST00000477868.1:n.232A>G
NM_024529.4:c.1520A>G , LRG_507t1:c.1520A>G	NP_078805.3:p.Asp507Gly
NM_024529.5:c.1520A>G MANE Select	NP_078805.3:p.Asp507Gly