Canonical Allele Identifier: CA2844915333

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122187C>A , CM000663.2:g.193122187C>A	GRCh38
NC_000001.10:g.193091317C>A , CM000663.1:g.193091317C>A	GRCh37
NC_000001.9:g.191357940C>A	NCBI36
NG_012691.1:g.5230C>A , LRG_507:g.5230C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-14C>A MANE Select	ENSP00000356405.4:n.-14C>A
ENST00000635846.1:c.-14C>A	ENSP00000490035.1:n.-14C>A
ENST00000643006.1:c.-14C>A	ENSP00000496633.1:n.-14C>A
ENST00000643784.1:c.-14C>A	ENSP00000494944.1:n.-14C>A
ENST00000648071.1:c.-14C>A	ENSP00000497513.1:n.-14C>A
ENST00000649895.1:n.205C>A
ENST00000650197.1:c.-14C>A	ENSP00000496929.1:n.-14C>A
ENST00000367435.3:c.-14C>A	ENSP00000356405.3:n.-14C>A
NM_024529.4:c.-14C>A , LRG_507t1:c.-14C>A	NP_078805.3:n.-14C>A
XM_006711537.2:c.-14C>A	XP_006711600.1:n.-14C>A
XM_006711537.4:c.-14C>A	XP_006711600.1:n.-14C>A
XR_001738350.1:n.1470G>T
NM_024529.5:c.-14C>A MANE Select	NP_078805.3:n.-14C>A