Canonical Allele Identifier: CA1010608166

Gene: CDC73

Linked Data

• dbSNP Id: rs1675458847
• gnomAD v3: 1-193122120-GGGCGA-G
• gnomAD v4: 1-193122120-GGGCGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122126_193122130del , CM000663.2:g.193122126_193122130del	GRCh38
NC_000001.10:g.193091256_193091260del , CM000663.1:g.193091256_193091260del	GRCh37
NC_000001.9:g.191357879_191357883del	NCBI36
NG_012691.1:g.5169_5173del , LRG_507:g.5169_5173del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-75_-71del MANE Select	ENSP00000356405.4:n.-75_-71del
ENST00000643006.1:c.-75_-71del	ENSP00000496633.1:n.-75_-71del
ENST00000649895.1:n.144_148del
ENST00000650197.1:c.-75_-71del	ENSP00000496929.1:n.-75_-71del
ENST00000367435.3:c.-75_-71del	ENSP00000356405.3:n.-75_-71del
NM_024529.4:c.-75_-71del , LRG_507t1:c.-75_-71del	NP_078805.3:n.-75_-71del
XM_006711537.2:c.-75_-71del	XP_006711600.1:n.-75_-71del
XM_006711537.4:c.-75_-71del	XP_006711600.1:n.-75_-71del
XR_001738350.1:n.1532_1536del
NM_024529.5:c.-75_-71del MANE Select	NP_078805.3:n.-75_-71del