Canonical Allele Identifier: CA2747147004
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193203574_193203593del , CM000663.2:g.193203574_193203593del GRCh38
NC_000001.10:g.193172704_193172723del , CM000663.1:g.193172704_193172723del GRCh37
NC_000001.9:g.191439327_191439346del NCBI36
NG_012691.1:g.86617_86636del , LRG_507:g.86617_86636del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.973-221_973-202del MANE Select ENSP00000356405.4:n.973-221_973-202del
ENST00000635846.1:c.730-221_730-202del ENSP00000490035.1:n.730-221_730-202del
ENST00000643006.1:c.1041-221_1041-202del ENSP00000496633.1:n.1041-221_1041-202del
ENST00000648071.1:c.*949-221_*949-202del ENSP00000497513.1:n.*949-221_*949-202del
ENST00000649613.1:n.223-221_223-202del
ENST00000649895.1:n.1191-221_1191-202del
ENST00000650197.1:c.973-221_973-202del ENSP00000496929.1:n.973-221_973-202del
ENST00000367435.3:c.973-221_973-202del ENSP00000356405.3:n.973-221_973-202del
NM_024529.4:c.973-221_973-202del , LRG_507t1:c.973-221_973-202del NP_078805.3:n.973-221_973-202del
NM_024529.5:c.973-221_973-202del MANE Select NP_078805.3:n.973-221_973-202del