Canonical Allele Identifier: CA1216113341

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122130A= , CM000663.2:g.193122130A=	GRCh38
NC_000001.10:g.193091260A= , CM000663.1:g.193091260A=	GRCh37
NC_000001.9:g.191357883A=	NCBI36
NG_012691.1:g.5173A= , LRG_507:g.5173A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-71A= MANE Select	ENSP00000356405.4:n.-71A=
ENST00000643006.1:c.-71A=	ENSP00000496633.1:n.-71A=
ENST00000643784.1:c.-71A=	ENSP00000494944.1:n.-71A=
ENST00000649895.1:n.148A=
ENST00000650197.1:c.-71A=	ENSP00000496929.1:n.-71A=
ENST00000367435.3:c.-71A=	ENSP00000356405.3:n.-71A=
NM_024529.4:c.-71A= , LRG_507t1:c.-71A=	NP_078805.3:n.-71A=
XM_006711537.2:c.-71A=	XP_006711600.1:n.-71A=
XM_006711537.4:c.-71A=	XP_006711600.1:n.-71A=
XR_001738350.1:n.1527T=
NM_024529.5:c.-71A= MANE Select	NP_078805.3:n.-71A=