UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
COSMIC:
COSM29474
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.171410544_171410545delinsCTGGAG , CM000667.2:g.171410544_171410545delinsCTGGAG | GRCh38 |
| NC_000005.9:g.170837548_170837549delinsCTGGAG , CM000667.1:g.170837548_170837549delinsCTGGAG | GRCh37 |
| NC_000005.8:g.170770153_170770154delinsCTGGAG | NCBI36 |
| NG_016018.1:g.27841_27842delinsCTGGAG , LRG_458:g.27841_27842delinsCTGGAG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000296930.10:c.864_865delinsCTGGAG MANE Select | ENSP00000296930.5:p.Trp288CysfsTer12 | |
| ENST00000518587.2:n.1058_1059delinsCTGGAG | ||
| ENST00000521260.2:n.1242_1243delinsCTGGAG | ||
| ENST00000521672.6:c.672_673delinsCTGGAG | ENSP00000429485.2:p.Trp224CysfsTer12 | |
| ENST00000676504.1:n.1610_1611delinsCTGGAG | ||
| ENST00000676589.1:c.951_952delinsCTGGAG | ENSP00000503283.1:p.Trp317CysfsTer12 | |
| ENST00000676613.1:c.*1611_*1612delinsCTGGAG | ENSP00000503767.1:n.*1611_*1612delinsCTGG... | |
| ENST00000676625.1:n.3281_3282delinsCTGGAG | ||
| ENST00000677297.1:c.351_352delinsCTGGAG | ENSP00000504016.1:p.Trp117CysfsTer12 | |
| ENST00000677325.1:c.672_673delinsCTGGAG | ENSP00000503781.1:p.Trp224CysfsTer12 | |
| ENST00000677357.1:c.897_898delinsCTGGAG | ENSP00000504740.1:p.Trp299CysfsTer12 | |
| ENST00000677467.1:n.2289_2290delinsCTGGAG | ||
| ENST00000677600.1:n.2182_2183delinsCTGGAG | ||
| ENST00000677672.1:n.2287_2288delinsCTGGAG | ||
| ENST00000677682.1:n.2194_2195delinsCTGGAG | ||
| ENST00000677741.1:n.2130_2131delinsCTGGAG | ||
| ENST00000677904.1:n.1140_1141delinsCTGGAG | ||
| ENST00000677907.1:c.585_586delinsCTGGAG | ENSP00000504308.1:p.Trp195CysfsTer12 | |
| ENST00000678186.1:n.2334_2335delinsCTGGAG | ||
| ENST00000678267.1:c.*1965_*1966delinsCTGGAG | ENSP00000504107.1:n.*1965_*1966delinsCTGG... | |
| ENST00000678280.1:c.*849_*850delinsCTGGAG | ENSP00000503235.1:n.*849_*850delinsCTGGAG... | |
| ENST00000678774.1:c.*340_*341delinsCTGGAG | ENSP00000503150.1:n.*340_*341delinsCTGGAG... | |
| ENST00000679190.1:c.*47_*48delinsCTGGAG | ENSP00000503408.1:n.*47_*48delinsCTGGAG | |
| ENST00000296930.9:c.864_865delinsCTGGAG | ENSP00000296930.5:p.Trp288CysfsTer12 | |
| ENST00000351986.10:c.777_778delinsCTGGAG | ENSP00000341168.6:p.Trp259CysfsTer12 | |
| ENST00000517671.5:c.864_865delinsCTGGAG | ENSP00000428755.1:p.Trp288CysfsTer12 | |
| ENST00000524204.1:n.300_301delinsCTGGAG | ||
| NM_002520.6:c.864_865delinsCTGGAG , LRG_458t1:c.864_865delinsCTGGAG | NP_002511.1:p.Trp288CysfsTer12 | |
| NM_199185.3:c.777_778delinsCTGGAG | NP_954654.1:p.Trp259CysfsTer12 | |
| XM_011534564.1:c.672_673delinsCTGGAG | XP_011532866.1:p.Trp224CysfsTer12 | |
| NM_001355006.1:c.864_865delinsCTGGAG | NP_001341935.1:p.Trp288CysfsTer12 | |
| NM_001355007.1:c.672_673delinsCTGGAG | NP_001341936.1:p.Trp224CysfsTer12 | |
| NM_001355010.1:c.483_484delinsCTGGAG | NP_001341939.1:p.Trp161CysfsTer12 | |
| NR_149149.1:n.981_982delinsCTGGAG | ||
| NM_001355006.2:c.864_865delinsCTGGAG | NP_001341935.1:p.Trp288CysfsTer12 | |
| NM_001355007.2:c.672_673delinsCTGGAG | NP_001341936.1:p.Trp224CysfsTer12 | |
| NM_001355010.2:c.483_484delinsCTGGAG | NP_001341939.1:p.Trp161CysfsTer12 | |
| NM_002520.7:c.864_865delinsCTGGAG MANE Select | NP_002511.1:p.Trp288CysfsTer12 | |
| NM_199185.4:c.777_778delinsCTGGAG | NP_954654.1:p.Trp259CysfsTer12 | |
| NR_149149.2:n.836_837delinsCTGGAG |