Canonical Allele Identifier: CA528019094
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1467021185
gnomAD v2: 1-193220543-C-CA
gnomAD v3: 1-193251413-C-CA
gnomAD v4: 1-193251413-C-CA
MyVariant Identifiers: chr1:g.193220543_193220544insA (hg19) chr1:g.193251413_193251414insA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251414dup , CM000663.2:g.193251414dup GRCh38
NC_000001.10:g.193220544dup , CM000663.1:g.193220544dup GRCh37
NC_000001.9:g.191487167dup NCBI36
NG_012691.1:g.134457dup , LRG_507:g.134457dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*702dup MANE Select ENSP00000356405.4:n.*702dup
ENST00000635846.1:c.*702dup ENSP00000490035.1:n.*702dup
ENST00000643006.1:c.*1208dup ENSP00000496633.1:n.*1208dup
ENST00000367435.3:c.*702dup ENSP00000356405.3:n.*702dup
NM_024529.4:c.*702dup , LRG_507t1:c.*702dup NP_078805.3:n.*702dup
NM_024529.5:c.*702dup MANE Select NP_078805.3:n.*702dup
Search 100 bp 5'
Search 100 bp 3'