Canonical Allele Identifier: CA2580061753

Gene: CDC73

Linked Data

• ClinVar Variation Id: 1768030
• ClinVar RCV Id: RCV002376741

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203790T>G , CM000663.2:g.193203790T>G	GRCh38
NC_000001.10:g.193172920T>G , CM000663.1:g.193172920T>G	GRCh37
NC_000001.9:g.191439543T>G	NCBI36
NG_012691.1:g.86833T>G , LRG_507:g.86833T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-5T>G MANE Select	ENSP00000356405.4:n.973-5T>G
ENST00000635846.1:c.730-5T>G	ENSP00000490035.1:n.730-5T>G
ENST00000643006.1:c.1041-5T>G	ENSP00000496633.1:n.1041-5T>G
ENST00000648071.1:c.*949-5T>G	ENSP00000497513.1:n.*949-5T>G
ENST00000649613.1:n.223-5T>G
ENST00000649895.1:n.1191-5T>G
ENST00000650197.1:c.973-5T>G	ENSP00000496929.1:n.973-5T>G
ENST00000367435.3:c.973-5T>G	ENSP00000356405.3:n.973-5T>G
NM_024529.4:c.973-5T>G , LRG_507t1:c.973-5T>G	NP_078805.3:n.973-5T>G
NM_024529.5:c.973-5T>G MANE Select	NP_078805.3:n.973-5T>G