Canonical Allele Identifier: CA2649624659
Gene: CDC73 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122125_193122152dup , CM000663.2:g.193122125_193122152dup GRCh38
NC_000001.10:g.193091255_193091282dup , CM000663.1:g.193091255_193091282dup GRCh37
NC_000001.9:g.191357878_191357905dup NCBI36
NG_012691.1:g.5168_5195dup , LRG_507:g.5168_5195dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-76_-49dup MANE Select ENSP00000356405.4:n.-76_-49dup
ENST00000643006.1:c.-76_-49dup ENSP00000496633.1:n.-76_-49dup
ENST00000649895.1:n.143_170dup
ENST00000650197.1:c.-76_-49dup ENSP00000496929.1:n.-76_-49dup
ENST00000367435.3:c.-76_-49dup ENSP00000356405.3:n.-76_-49dup
NM_024529.4:c.-76_-49dup , LRG_507t1:c.-76_-49dup NP_078805.3:n.-76_-49dup
XM_006711537.2:c.-76_-49dup XP_006711600.1:n.-76_-49dup
XM_006711537.4:c.-76_-49dup XP_006711600.1:n.-76_-49dup
XR_001738350.1:n.1509_1536dup
NM_024529.5:c.-76_-49dup MANE Select NP_078805.3:n.-76_-49dup