Canonical Allele Identifier: CA2649624645
Gene: CDC73 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122113_193122146del , CM000663.2:g.193122113_193122146del GRCh38
NC_000001.10:g.193091243_193091276del , CM000663.1:g.193091243_193091276del GRCh37
NC_000001.9:g.191357866_191357899del NCBI36
NG_012691.1:g.5156_5189del , LRG_507:g.5156_5189del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-88_-55del MANE Select ENSP00000356405.4:n.-88_-55del
ENST00000643006.1:c.-88_-55del ENSP00000496633.1:n.-88_-55del
ENST00000649895.1:n.131_164del
ENST00000650197.1:c.-88_-55del ENSP00000496929.1:n.-88_-55del
ENST00000367435.3:c.-88_-55del ENSP00000356405.3:n.-88_-55del
NM_024529.4:c.-88_-55del , LRG_507t1:c.-88_-55del NP_078805.3:n.-88_-55del
XM_006711537.2:c.-88_-55del XP_006711600.1:n.-88_-55del
XM_006711537.4:c.-88_-55del XP_006711600.1:n.-88_-55del
XR_001738350.1:n.1517_1550del
NM_024529.5:c.-88_-55del MANE Select NP_078805.3:n.-88_-55del