Canonical Allele Identifier: CA344076187

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193172980C>G (hg19) ; chr1:g.193203850C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203850C>G , CM000663.2:g.193203850C>G	GRCh38
NC_000001.10:g.193172980C>G , CM000663.1:g.193172980C>G	GRCh37
NC_000001.9:g.191439603C>G	NCBI36
NG_012691.1:g.86893C>G , LRG_507:g.86893C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1028C>G MANE Select	ENSP00000356405.4:p.Pro343Arg
ENST00000635846.1:c.785C>G	ENSP00000490035.1:p.Pro262Arg
ENST00000643006.1:c.1096C>G	ENSP00000496633.1:p.Gln366Glu
ENST00000648071.1:c.*1004C>G	ENSP00000497513.1:n.*1004C>G
ENST00000649613.1:n.278C>G
ENST00000649895.1:n.1246C>G
ENST00000650197.1:c.1028C>G	ENSP00000496929.1:p.Pro343Arg
ENST00000367435.3:c.1028C>G	ENSP00000356405.3:p.Pro343Arg
NM_024529.4:c.1028C>G , LRG_507t1:c.1028C>G	NP_078805.3:p.Pro343Arg
NM_024529.5:c.1028C>G MANE Select	NP_078805.3:p.Pro343Arg