Linked Data
dbSNP Id:
rs1322925717
gnomAD v2:
5-54466553-C-CCTACCTG
gnomAD v4:
5-55170725-C-CCTACCTG
MyVariant Identifiers:
chr5:g.54466553_54466554insCTACCTG (hg19)
chr5:g.55170725_55170726insCTACCTG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.55170726_55170732dup , CM000667.2:g.55170726_55170732dup | GRCh38 |
| NC_000005.9:g.54466554_54466560dup , CM000667.1:g.54466554_54466560dup | GRCh37 |
| NC_000005.8:g.54502311_54502317dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381375.7:c.126+1856_126+1862dup (CDC20B) MANE Select | ENSP00000370781.2:n.126+1856_126+1862dup | |
| ENST00000296733.5:c.126+1856_126+1862dup (CDC20B) | ENSP00000296733.1:n.126+1856_126+1862dup | |
| ENST00000322374.10:c.126+1856_126+1862dup (CDC20B) | ENSP00000315720.6:n.126+1856_126+1862dup | |
| ENST00000381375.6:c.126+1856_126+1862dup (CDC20B) | ENSP00000370781.2:n.126+1856_126+1862dup | |
| ENST00000507931.1:c.63+2206_63+2212dup (CDC20B) | ENSP00000423919.1:n.63+2206_63+2212dup | |
| ENST00000513180.5:c.126+1856_126+1862dup (CDC20B) | ENSP00000426776.1:n.126+1856_126+1862dup | |
| NM_001145734.2:c.126+1856_126+1862dup (CDC20B) | NP_001139206.2:n.126+1856_126+1862dup | |
| NM_001170402.1:c.126+1856_126+1862dup (CDC20B) MANE Select | NP_001163873.1:n.126+1856_126+1862dup | |
| NM_152623.2:c.126+1856_126+1862dup (CDC20B) | NP_689836.2:n.126+1856_126+1862dup | |
| NR_030387.1:n.11_17dup (MIR449B) | ||
| XM_011543218.1:c.126+1856_126+1862dup (CDC20B) | XP_011541520.1:n.126+1856_126+1862dup | |
| XM_011543218.2:c.126+1856_126+1862dup (CDC20B) | XP_011541520.1:n.126+1856_126+1862dup |