Canonical Allele Identifier: CA2747147006

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203669_193203681dup , CM000663.2:g.193203669_193203681dup	GRCh38
NC_000001.10:g.193172799_193172811dup , CM000663.1:g.193172799_193172811dup	GRCh37
NC_000001.9:g.191439422_191439434dup	NCBI36
NG_012691.1:g.86712_86724dup , LRG_507:g.86712_86724dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-126_973-114dup MANE Select	ENSP00000356405.4:n.973-126_973-114dup
ENST00000635846.1:c.730-126_730-114dup	ENSP00000490035.1:n.730-126_730-114dup
ENST00000643006.1:c.1041-126_1041-114dup	ENSP00000496633.1:n.1041-126_1041-114dup
ENST00000648071.1:c.*949-126_*949-114dup	ENSP00000497513.1:n.*949-126_*949-114dup
ENST00000649613.1:n.223-126_223-114dup
ENST00000649895.1:n.1191-126_1191-114dup
ENST00000650197.1:c.973-126_973-114dup	ENSP00000496929.1:n.973-126_973-114dup
ENST00000367435.3:c.973-126_973-114dup	ENSP00000356405.3:n.973-126_973-114dup
NM_024529.4:c.973-126_973-114dup , LRG_507t1:c.973-126_973-114dup	NP_078805.3:n.973-126_973-114dup
NM_024529.5:c.973-126_973-114dup MANE Select	NP_078805.3:n.973-126_973-114dup