Canonical Allele Identifier: CA2649624549

Gene: CDC73

Linked Data

• gnomAD v4: 1-193122031-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122032dup , CM000663.2:g.193122032dup	GRCh38
NC_000001.10:g.193091162dup , CM000663.1:g.193091162dup	GRCh37
NC_000001.9:g.191357785dup	NCBI36
NG_012691.1:g.5075dup , LRG_507:g.5075dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000367435.5:c.-169dup MANE Select	ENSP00000356405.4:n.-169dup
ENST00000643006.1:c.-169dup	ENSP00000496633.1:n.-169dup
ENST00000649895.1:n.50dup
ENST00000367435.3:c.-169dup	ENSP00000356405.3:n.-169dup
NM_024529.4:c.-169dup , LRG_507t1:c.-169dup	NP_078805.3:n.-169dup
XM_006711537.4:c.-169dup	XP_006711600.1:n.-169dup
XR_001738350.1:n.1625dup
NM_024529.5:c.-169dup MANE Select	NP_078805.3:n.-169dup