Canonical Allele Identifier: CA1216113278

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122033T= , CM000663.2:g.193122033T=	GRCh38
NC_000001.10:g.193091163T= , CM000663.1:g.193091163T=	GRCh37
NC_000001.9:g.191357786T=	NCBI36
NG_012691.1:g.5076T= , LRG_507:g.5076T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-168T= MANE Select	ENSP00000356405.4:n.-168T=
ENST00000643006.1:c.-168T=	ENSP00000496633.1:n.-168T=
ENST00000649895.1:n.51T=
ENST00000367435.3:c.-168T=	ENSP00000356405.3:n.-168T=
NM_024529.4:c.-168T= , LRG_507t1:c.-168T=	NP_078805.3:n.-168T=
XM_006711537.4:c.-168T=	XP_006711600.1:n.-168T=
XR_001738350.1:n.1624A=
NM_024529.5:c.-168T= MANE Select	NP_078805.3:n.-168T=