Canonical Allele Identifier: CA1216113338

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122126G= , CM000663.2:g.193122126G=	GRCh38
NC_000001.10:g.193091256G= , CM000663.1:g.193091256G=	GRCh37
NC_000001.9:g.191357879G=	NCBI36
NG_012691.1:g.5169G= , LRG_507:g.5169G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-75G= MANE Select	ENSP00000356405.4:n.-75G=
ENST00000643006.1:c.-75G=	ENSP00000496633.1:n.-75G=
ENST00000643784.1:c.-75G=	ENSP00000494944.1:n.-75G=
ENST00000649895.1:n.144G=
ENST00000650197.1:c.-75G=	ENSP00000496929.1:n.-75G=
ENST00000367435.3:c.-75G=	ENSP00000356405.3:n.-75G=
NM_024529.4:c.-75G= , LRG_507t1:c.-75G=	NP_078805.3:n.-75G=
XM_006711537.2:c.-75G=	XP_006711600.1:n.-75G=
XM_006711537.4:c.-75G=	XP_006711600.1:n.-75G=
XR_001738350.1:n.1531C=
NM_024529.5:c.-75G= MANE Select	NP_078805.3:n.-75G=