Canonical Allele Identifier: CA2697811280
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs2103111208

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122072_193122073insAGCTGCTGCTGTTAG , CM000663.2:g.193122072_193122073insAGCTGCTGCTGTTAG GRCh38
NC_000001.10:g.193091202_193091203insAGCTGCTGCTGTTAG , CM000663.1:g.193091202_193091203insAGCTGCTGCTGTTAG GRCh37
NC_000001.9:g.191357825_191357826insAGCTGCTGCTGTTAG NCBI36
NG_012691.1:g.5115_5116insAGCTGCTGCTGTTAG , LRG_507:g.5115_5116insAGCTGCTGCTGTTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-129_-128insAGCTGCTGCTGTTAG MANE Select ENSP00000356405.4:n.-129_-128insAGCTGCTGCTGTTAG
ENST00000643006.1:c.-129_-128insAGCTGCTGCTGTTAG ENSP00000496633.1:n.-129_-128insAGCTGCTGCTGTTAG
ENST00000649895.1:n.90_91insAGCTGCTGCTGTTAG
ENST00000367435.3:c.-129_-128insAGCTGCTGCTGTTAG ENSP00000356405.3:n.-129_-128insAGCTGCTGCTGTTAG
NM_024529.4:c.-129_-128insAGCTGCTGCTGTTAG , LRG_507t1:c.-129_-128insAGCTGCTGCTGTTAG NP_078805.3:n.-129_-128insAGCTGCTGCTGTTAG
XM_006711537.2:c.-129_-128insAGCTGCTGCTGTTAG XP_006711600.1:n.-129_-128insAGCTGCTGCTGTTAG
XM_006711537.4:c.-129_-128insAGCTGCTGCTGTTAG XP_006711600.1:n.-129_-128insAGCTGCTGCTGTTAG
XR_001738350.1:n.1592_1593insAGCAGCTCTAACAGC
NM_024529.5:c.-129_-128insAGCTGCTGCTGTTAG MANE Select NP_078805.3:n.-129_-128insAGCTGCTGCTGTTAG