Linked Data
ClinVar Variation Id:
433934
dbSNP Id:
rs761468459
ExAC:
1:45797911 GC / G
gnomAD v2:
1-45797911-GC-G
gnomAD v3:
1-45332239-GC-G
gnomAD v4:
1-45332239-GC-G
PubMed:
PMID:16557584
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45332243del , CM000663.2:g.45332243del | GRCh38 |
| NC_000001.10:g.45797915del , CM000663.1:g.45797915del | GRCh37 |
| NC_000001.9:g.45570502del | NCBI36 |
| NG_008189.1:g.13231del , LRG_220:g.13231del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000412971.6:c.391del | ENSP00000410263.2:p.Ala131ProfsTer? | |
| ENST00000435155.2:c.808del | ENSP00000403655.2:p.Ala270ProfsTer? | |
| ENST00000467459.6:c.775del | ENSP00000435889.2:p.Ala259ProfsTer? | |
| ENST00000483127.2:c.793del | ENSP00000436469.2:p.Ala265ProfsTer? | |
| ENST00000485271.6:c.775del | ENSP00000431264.2:p.Ala259ProfsTer? | |
| ENST00000529892.6:c.817del | ENSP00000432528.2:p.Ala273ProfsTer? | |
| ENST00000533178.6:c.*104del | ENSP00000436430.2:n.*104del | |
| ENST00000672314.2:c.775del | ENSP00000500828.2:p.Ala259ProfsTer? | |
| ENST00000674679.2:c.*687del | ENSP00000501623.2:n.*687del | |
| ENST00000710952.2:c.859del MANE Plus Clinical | ENSP00000518552.2:p.Ala287ProfsTer? | |
| ENST00000672818.3:c.850del | ENSP00000500891.1:p.Ala284ProfsTer? | |
| ENST00000450313.6:c.*104del | ENSP00000408176.2:n.*104del | |
| ENST00000456914.7:c.775del MANE Select | ENSP00000407590.2:p.Ala259ProfsTer? | |
| ENST00000461495.6:c.*514del | ENSP00000437166.1:n.*514del | |
| ENST00000671898.1:c.1363del | ENSP00000499896.1:p.Ala455ProfsTer? | |
| ENST00000672011.1:c.*104del | ENSP00000500418.1:n.*104del | |
| ENST00000672314.1:c.775del | ENSP00000500828.1:p.Ala259ProfsTer? | |
| ENST00000672593.1:c.*828del | ENSP00000500455.1:n.*828del | |
| ENST00000672764.1:c.*104del | ENSP00000500886.1:n.*104del | |
| ENST00000672818.2:c.850del | ENSP00000500891.1:p.Ala284ProfsTer? | |
| ENST00000673134.1:c.*472del | ENSP00000500526.1:n.*472del | |
| ENST00000674679.1:c.803del | ENSP00000501623.1:n.803del | |
| ENST00000354383.10:c.778del | ENSP00000346354.6:p.Ala260ProfsTer? | |
| ENST00000355498.6:c.775del | ENSP00000347685.2:p.Ala259ProfsTer? | |
| ENST00000372098.7:c.850del | ENSP00000361170.3:p.Ala284ProfsTer? | |
| ENST00000372104.5:c.775del | ENSP00000361176.1:p.Ala259ProfsTer? | |
| ENST00000372110.7:c.820del | ENSP00000361182.3:p.Ala274ProfsTer? | |
| ENST00000372115.7:c.817del | ENSP00000361187.3:p.Ala273ProfsTer? | |
| ENST00000412971.5:c.391del | ENSP00000410263.1:p.Ala131ProfsTer? | |
| ENST00000435155.1:c.808del | ENSP00000403655.1:p.Ala270ProfsTer? | |
| ENST00000448481.5:c.808del | ENSP00000409718.1:p.Ala270ProfsTer? | |
| ENST00000450313.5:c.859del | ENSP00000408176.1:p.Ala287ProfsTer? | |
| ENST00000456914.6:c.775del | ENSP00000407590.2:p.Ala259ProfsTer? | |
| ENST00000461495.5:c.*514del | ENSP00000437166.1:n.*514del | |
| ENST00000462388.5:n.466del | ||
| ENST00000466231.1:n.140del | ||
| ENST00000467459.5:c.169del | ENSP00000435889.1:p.Ala57ProfsTer? | |
| ENST00000467940.5:c.*698del | ENSP00000436478.1:n.*698del | |
| ENST00000470256.5:c.*104del | ENSP00000434985.1:n.*104del | |
| ENST00000475516.5:c.*588del | ENSP00000433843.1:n.*588del | |
| ENST00000478796.5:n.762del | ||
| ENST00000481571.5:c.*588del | ENSP00000436597.1:n.*588del | |
| ENST00000488731.6:c.187+523del | ENSP00000432330.1:n.187+523del | |
| ENST00000528013.6:c.817del | ENSP00000433130.2:p.Ala273ProfsTer? | |
| ENST00000529892.5:c.39del | ||
| ENST00000529984.5:c.187+523del | ENSP00000437093.1:n.187+523del | |
| ENST00000531105.5:c.115+2151del | ENSP00000431292.1:n.115+2151del | |
| ENST00000533178.5:c.404del | ENSP00000436430.1:n.404del | |
| NM_001048171.1:c.817del | NP_001041636.1:p.Ala273ProfsTer? | |
| NM_001048172.1:c.778del | NP_001041637.1:p.Ala260ProfsTer? | |
| NM_001048173.1:c.775del | NP_001041638.1:p.Ala259ProfsTer? | |
| NM_001048174.1:c.775del | NP_001041639.1:p.Ala259ProfsTer? | |
| NM_001128425.1:c.859del , LRG_220t1:c.859del | NP_001121897.1:p.Ala287ProfsTer? | |
| NM_001293190.1:c.820del | NP_001280119.1:p.Ala274ProfsTer? | |
| NM_001293191.1:c.808del | NP_001280120.1:p.Ala270ProfsTer? | |
| NM_001293192.1:c.499del | NP_001280121.1:p.Ala167ProfsTer? | |
| NM_001293195.1:c.775del | NP_001280124.1:p.Ala259ProfsTer? | |
| NM_001293196.1:c.499del | NP_001280125.1:p.Ala167ProfsTer? | |
| NM_012222.2:c.850del | NP_036354.1:p.Ala284ProfsTer? | |
| XM_011541497.1:c.835del | XP_011539799.1:p.Ala279ProfsTer? | |
| XM_011541498.1:c.817del | XP_011539800.1:p.Ala273ProfsTer? | |
| XM_011541499.1:c.817del | XP_011539801.1:p.Ala273ProfsTer? | |
| XM_011541500.1:c.817del | XP_011539802.1:p.Ala273ProfsTer? | |
| XM_011541501.1:c.817del | XP_011539803.1:p.Ala273ProfsTer? | |
| XM_011541502.1:c.817del | XP_011539804.1:p.Ala273ProfsTer? | |
| XM_011541503.1:c.817del | XP_011539805.1:p.Ala273ProfsTer? | |
| XM_011541504.1:c.808del | XP_011539806.1:p.Ala270ProfsTer? | |
| XM_011541505.1:c.397del | XP_011539807.1:p.Ala133ProfsTer? | |
| XM_011541506.1:c.397del | XP_011539808.1:p.Ala133ProfsTer? | |
| XM_011541507.1:c.388del | XP_011539809.1:p.Ala130ProfsTer? | |
| XM_011541508.1:c.403del | XP_011539810.1:p.Ala135ProfsTer? | |
| XR_946658.1:n.906del | ||
| NM_001350650.1:c.430del | NP_001337579.1:p.Ala144ProfsTer? | |
| NM_001350651.1:c.430del | NP_001337580.1:p.Ala144ProfsTer? | |
| NR_146882.1:n.1033del | ||
| NR_146883.1:n.847del | ||
| XM_011541497.3:c.835del | XP_011539799.1:p.Ala279ProfsTer? | |
| XM_011541500.3:c.817del | XP_011539802.1:p.Ala273ProfsTer? | |
| XM_011541501.2:c.817del | XP_011539803.1:p.Ala273ProfsTer? | |
| XM_011541502.2:c.817del | XP_011539804.1:p.Ala273ProfsTer? | |
| XM_011541503.2:c.817del | XP_011539805.1:p.Ala273ProfsTer? | |
| XM_011541504.2:c.808del | XP_011539806.1:p.Ala270ProfsTer? | |
| XM_011541505.2:c.397del | XP_011539807.1:p.Ala133ProfsTer? | |
| XM_011541506.2:c.397del | XP_011539808.1:p.Ala133ProfsTer? | |
| XM_017001331.1:c.817del | XP_016856820.1:p.Ala273ProfsTer? | |
| XM_017001332.1:c.817del | XP_016856821.1:p.Ala273ProfsTer? | |
| XM_017001333.1:c.817del | XP_016856822.1:p.Ala273ProfsTer? | |
| XM_017001334.1:c.778del | XP_016856823.1:p.Ala260ProfsTer? | |
| XM_017001335.1:c.499del | XP_016856824.1:p.Ala167ProfsTer? | |
| XM_017001336.1:c.430del | XP_016856825.1:p.Ala144ProfsTer? | |
| XM_017001337.1:c.430del | XP_016856826.1:p.Ala144ProfsTer? | |
| XM_024447244.1:c.430del | XP_024303012.1:p.Ala144ProfsTer? | |
| XM_024447245.1:c.430del | XP_024303013.1:p.Ala144ProfsTer? | |
| XM_024447248.1:c.388del | XP_024303016.1:p.Ala130ProfsTer? | |
| XM_024447249.1:c.259del | XP_024303017.1:p.Ala87ProfsTer? | |
| XM_024447250.1:c.259del | XP_024303018.1:p.Ala87ProfsTer? | |
| XM_024447251.1:c.259del | XP_024303019.1:p.Ala87ProfsTer? | |
| XR_001737190.1:n.820del | ||
| XR_001737192.1:n.632del | ||
| XR_002956643.1:n.812del | ||
| XR_002956644.1:n.1347del | ||
| XR_946658.2:n.920del | ||
| NM_001048171.2:c.775del | NP_001041636.2:p.Ala259ProfsTer? | |
| NM_001128425.2:c.859del MANE Plus Clinical | NP_001121897.1:p.Ala287ProfsTer? | |
| NM_001048172.2:c.778del | NP_001041637.1:p.Ala260ProfsTer? | |
| NM_001048173.2:c.775del | NP_001041638.1:p.Ala259ProfsTer? | |
| NM_001048174.2:c.775del MANE Select | NP_001041639.1:p.Ala259ProfsTer? | |
| NM_001293190.2:c.820del | NP_001280119.1:p.Ala274ProfsTer? | |
| NM_001293191.2:c.808del | NP_001280120.1:p.Ala270ProfsTer? | |
| NM_001293192.2:c.499del | NP_001280121.1:p.Ala167ProfsTer? | |
| NM_001293195.2:c.775del | NP_001280124.1:p.Ala259ProfsTer? | |
| NM_001293196.2:c.499del | NP_001280125.1:p.Ala167ProfsTer? | |
| NM_001350650.2:c.430del | NP_001337579.1:p.Ala144ProfsTer? | |
| NM_001350651.2:c.430del | NP_001337580.1:p.Ala144ProfsTer? | |
| NM_012222.3:c.850del | NP_036354.1:p.Ala284ProfsTer? | |
| NR_146882.2:n.1003del | ||
| NR_146883.2:n.852del |