Linked Data
ClinVar Variation Id:
183277
dbSNP Id:
rs730882198
gnomAD v4:
13-36314259-G-GT
MyVariant Identifiers:
chr13:g.36888397dupT (hg19)
chr13:g.36888396_36888397insT (hg19)
chr13:g.36314260dupT (hg38)
chr13:g.36314259_36314260insT (hg38)
PubMed:
PMID:25558065
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.36314260dup , CM000675.2:g.36314260dup | GRCh38 |
| NC_000013.10:g.36888397dup , CM000675.1:g.36888397dup | GRCh37 |
| NC_000013.9:g.35786397dup | NCBI36 |
| NG_011559.1:g.60921dup | |
| NG_011559.2:g.60921dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000438666.7:c.1450dup MANE Select | ENSP00000406061.2:p.Thr484AsnfsTer13 | |
| ENST00000650221.1:c.1450dup | ENSP00000497209.1:p.Thr484AsnfsTer13 | |
| ENST00000355182.8:c.1450dup | ENSP00000347314.4:p.Thr484AsnfsTer13 | |
| ENST00000438666.6:c.1450dup | ENSP00000406061.2:p.Thr484AsnfsTer13 | |
| ENST00000451493.5:c.1450dup | ENSP00000414147.1:p.Thr484AsnfsTer13 | |
| ENST00000475603.5:n.211dup | ||
| ENST00000482146.1:n.182dup | ||
| ENST00000494062.2:c.1450dup | ENSP00000473599.1:p.Thr484AsnfsTer13 | |
| NM_001142294.1:c.1450dup | NP_001135766.1:p.Thr484AsnfsTer13 | |
| NM_001142295.1:c.1450dup | NP_001135767.1:p.Thr484AsnfsTer13 | |
| NM_001142296.1:c.1450dup | NP_001135768.1:p.Thr484AsnfsTer13 | |
| NM_015087.4:c.1450dup | NP_055902.1:p.Thr484AsnfsTer13 | |
| XM_005266313.3:c.1450dup | XP_005266370.1:p.Thr484AsnfsTer13 | |
| XM_005266314.2:c.1450dup | XP_005266371.1:p.Thr484AsnfsTer13 | |
| XM_005266315.2:c.1450dup | XP_005266372.1:p.Thr484AsnfsTer13 | |
| XM_005266316.2:c.1450dup | XP_005266373.1:p.Thr484AsnfsTer13 | |
| XM_005266317.2:c.1450dup | XP_005266374.1:p.Thr484AsnfsTer13 | |
| XM_011535012.1:c.1450dup | XP_011533314.1:p.Thr484AsnfsTer13 | |
| XR_941540.1:n.1712dup | ||
| XM_005266313.5:c.1450dup | XP_005266370.1:p.Thr484AsnfsTer13 | |
| XM_005266314.3:c.1450dup | XP_005266371.1:p.Thr484AsnfsTer13 | |
| XM_005266315.3:c.1450dup | XP_005266372.1:p.Thr484AsnfsTer13 | |
| XM_005266317.3:c.1450dup | XP_005266374.1:p.Thr484AsnfsTer13 | |
| XM_011535012.2:c.1450dup | XP_011533314.1:p.Thr484AsnfsTer13 | |
| XM_024449334.1:c.1450dup | XP_024305102.1:p.Thr484AsnfsTer13 | |
| XR_001749523.2:n.1678dup | ||
| NM_015087.5:c.1450dup MANE Select | NP_055902.1:p.Thr484AsnfsTer13 | |
| NM_001142296.2:c.1450dup | NP_001135768.1:p.Thr484AsnfsTer13 | |
| NM_001142294.2:c.1450dup | NP_001135766.1:p.Thr484AsnfsTer13 | |
| NM_001142295.2:c.1450dup | NP_001135767.1:p.Thr484AsnfsTer13 |