Canonical Allele Identifier: CA35103570
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs761880826
MyVariant Identifiers: chr1:g.193220692_193220693insT (hg19) chr1:g.193251562_193251563insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251566dup , CM000663.2:g.193251566dup GRCh38
NC_000001.10:g.193220696dup , CM000663.1:g.193220696dup GRCh37
NC_000001.9:g.191487319dup NCBI36
NG_012691.1:g.134609dup , LRG_507:g.134609dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*854dup MANE Select ENSP00000356405.4:n.*854dup
ENST00000635846.1:c.*854dup ENSP00000490035.1:n.*854dup
ENST00000643006.1:c.*1360dup ENSP00000496633.1:n.*1360dup
ENST00000367435.3:c.*854dup ENSP00000356405.3:n.*854dup
NM_024529.4:c.*854dup , LRG_507t1:c.*854dup NP_078805.3:n.*854dup
NM_024529.5:c.*854dup MANE Select NP_078805.3:n.*854dup
Search 100 bp 5'
Search 100 bp 3'