Canonical Allele Identifier: CA2649598688

Gene: CDC73

Linked Data

• gnomAD v4: 1-193203655-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203657dup , CM000663.2:g.193203657dup	GRCh38
NC_000001.10:g.193172787dup , CM000663.1:g.193172787dup	GRCh37
NC_000001.9:g.191439410dup	NCBI36
NG_012691.1:g.86700dup , LRG_507:g.86700dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-138dup MANE Select	ENSP00000356405.4:n.973-138dup
ENST00000635846.1:c.730-138dup	ENSP00000490035.1:n.730-138dup
ENST00000643006.1:c.1041-138dup	ENSP00000496633.1:n.1041-138dup
ENST00000648071.1:c.*949-138dup	ENSP00000497513.1:n.*949-138dup
ENST00000649613.1:n.223-138dup
ENST00000649895.1:n.1191-138dup
ENST00000650197.1:c.973-138dup	ENSP00000496929.1:n.973-138dup
ENST00000367435.3:c.973-138dup	ENSP00000356405.3:n.973-138dup
NM_024529.4:c.973-138dup , LRG_507t1:c.973-138dup	NP_078805.3:n.973-138dup
NM_024529.5:c.973-138dup MANE Select	NP_078805.3:n.973-138dup