Canonical Allele Identifier: CA1216113282
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122037_193122038delinsGC , CM000663.2:g.193122037_193122038delinsGC GRCh38
NC_000001.10:g.193091167_193091168delinsGC , CM000663.1:g.193091167_193091168delinsGC GRCh37
NC_000001.9:g.191357790_191357791delinsGC NCBI36
NG_012691.1:g.5080_5081delinsGC , LRG_507:g.5080_5081delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-164_-163delinsGC MANE Select ENSP00000356405.4:n.-164_-163delinsGC
ENST00000643006.1:c.-164_-163delinsGC ENSP00000496633.1:n.-164_-163delinsGC
ENST00000649895.1:n.55_56delinsGC
ENST00000367435.3:c.-164_-163delinsGC ENSP00000356405.3:n.-164_-163delinsGC
NM_024529.4:c.-164_-163delinsGC , LRG_507t1:c.-164_-163delinsGC NP_078805.3:n.-164_-163delinsGC
XM_006711537.2:c.-164_-163delinsGC XP_006711600.1:n.-164_-163delinsGC
XM_006711537.4:c.-164_-163delinsGC XP_006711600.1:n.-164_-163delinsGC
XR_001738350.1:n.1619_1620delinsGC
NM_024529.5:c.-164_-163delinsGC MANE Select NP_078805.3:n.-164_-163delinsGC