Canonical Allele Identifier: CA2697810672
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs2103111104

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122011_193122012insCACGTACCCA , CM000663.2:g.193122011_193122012insCACGTACCCA GRCh38
NC_000001.10:g.193091141_193091142insCACGTACCCA , CM000663.1:g.193091141_193091142insCACGTACCCA GRCh37
NC_000001.9:g.191357764_191357765insCACGTACCCA NCBI36
NG_012691.1:g.5054_5055insCACGTACCCA , LRG_507:g.5054_5055insCACGTACCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000643006.1:c.-190_-189insCACGTACCCA ENSP00000496633.1:n.-190_-189insCACGTACCCA
ENST00000649895.1:n.29_30insCACGTACCCA
NM_024529.4:c.-190_-189insCACGTACCCA , LRG_507t1:c.-190_-189insCACGTACCCA NP_078805.3:n.-190_-189insCACGTACCCA
XR_001738350.1:n.1645_1646insTGGGTACGTG