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.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.88101084_88101089delinsGGATGT , CM000674.2:g.88101084_88101089delinsGGATGT | GRCh38 |
| NC_000012.11:g.88494861_88494866delinsGGATGT , CM000674.1:g.88494861_88494866delinsGGATGT | GRCh37 |
| NC_000012.10:g.87018992_87018997delinsGGATGT | NCBI36 |
| NG_008417.1:g.46128_46133delinsACATCC | |
| NG_008417.2:g.46128_46133delinsACATCC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000309041.12:c.2991+1749_2991+1754delinsACATCC | ENSP00000308021.8:n.2991+1749_2991+1754de... | |
| ENST00000547691.8:c.275+1749_275+1754delinsACATCC | ||
| ENST00000552810.6:c.2991+1749_2991+1754delinsACATCC MANE Select | ENSP00000448012.1:n.2991+1749_2991+1754de... | |
| ENST00000672414.2:c.*1162+1749_*1162+1754delinsACATCC | ENSP00000500729.1:n.*1162+1749_*1162+1754... | |
| ENST00000672647.1:n.1351+1749_1351+1754delinsACATCC | ||
| ENST00000673058.2:c.2991+1749_2991+1754delinsACATCC | ENSP00000500665.2:n.2991+1749_2991+1754de... | |
| ENST00000674971.1:c.2991+1749_2991+1754delinsACATCC | ENSP00000502194.1:n.2991+1749_2991+1754de... | |
| ENST00000675089.1:c.174+1749_174+1754delinsACATCC | ENSP00000501582.1:n.174+1749_174+1754deli... | |
| ENST00000675230.1:c.2970+1749_2970+1754delinsACATCC | ENSP00000502503.1:n.2970+1749_2970+1754de... | |
| ENST00000675408.1:c.2991+1749_2991+1754delinsACATCC | ENSP00000502298.1:n.2991+1749_2991+1754de... | |
| ENST00000675476.1:c.3852+1749_3852+1754delinsACATCC | ENSP00000502161.1:n.3852+1749_3852+1754de... | |
| ENST00000675628.1:n.3218+1749_3218+1754delinsACATCC | ||
| ENST00000675794.1:c.*1162+1749_*1162+1754delinsACATCC | ENSP00000502841.1:n.*1162+1749_*1162+1754... | |
| ENST00000675833.1:c.3759+1749_3759+1754delinsACATCC | ENSP00000502559.1:n.3759+1749_3759+1754de... | |
| ENST00000676074.1:c.2991+1749_2991+1754delinsACATCC | ENSP00000502079.1:n.2991+1749_2991+1754de... | |
| ENST00000676181.1:n.679+1749_679+1754delinsACATCC | ||
| ENST00000676363.1:n.8717+1749_8717+1754delinsACATCC | ||
| ENST00000676448.1:c.*904+1749_*904+1754delinsACATCC | ENSP00000501987.1:n.*904+1749_*904+1754de... | |
| ENST00000309041.11:c.2997+1749_2997+1754delinsACATCC | ENSP00000308021.7:n.2997+1749_2997+1754de... | |
| ENST00000547691.6:c.171+1749_171+1754delinsACATCC | ENSP00000446905.1:n.171+1749_171+1754deli... | |
| ENST00000552810.5:c.2991+1749_2991+1754delinsACATCC | ENSP00000448012.1:n.2991+1749_2991+1754de... | |
| ENST00000604024.5:c.2250+1749_2250+1754delinsACATCC | ENSP00000473863.1:n.2250+1749_2250+1754de... | |
| NM_025114.3:c.2991+1749_2991+1754delinsACATCC | NP_079390.3:n.2991+1749_2991+1754delinsAC... | |
| XM_011538756.1:c.3852+1749_3852+1754delinsACATCC | XP_011537058.1:n.3852+1749_3852+1754delin... | |
| XM_011538757.1:c.3852+1749_3852+1754delinsACATCC | XP_011537059.1:n.3852+1749_3852+1754delin... | |
| XM_011538758.1:c.3852+1749_3852+1754delinsACATCC | XP_011537060.1:n.3852+1749_3852+1754delin... | |
| XM_011538759.1:c.3852+1749_3852+1754delinsACATCC | XP_011537061.1:n.3852+1749_3852+1754delin... | |
| XM_011538760.1:c.3852+1749_3852+1754delinsACATCC | XP_011537062.1:n.3852+1749_3852+1754delin... | |
| XM_011538761.1:c.3852+1749_3852+1754delinsACATCC | XP_011537063.1:n.3852+1749_3852+1754delin... | |
| XM_011538762.1:c.3084+1749_3084+1754delinsACATCC | XP_011537064.1:n.3084+1749_3084+1754delin... | |
| XM_011538763.1:c.2991+1749_2991+1754delinsACATCC | XP_011537065.1:n.2991+1749_2991+1754delin... | |
| XM_011538764.1:c.3852+1749_3852+1754delinsACATCC | XP_011537066.1:n.3852+1749_3852+1754delin... | |
| XM_011538765.1:c.3852+1749_3852+1754delinsACATCC | XP_011537067.1:n.3852+1749_3852+1754delin... | |
| XM_011538766.1:c.2313+1749_2313+1754delinsACATCC | XP_011537068.1:n.2313+1749_2313+1754delin... | |
| XM_011538756.3:c.3852+1749_3852+1754delinsACATCC | XP_011537058.1:n.3852+1749_3852+1754delin... | |
| XM_011538757.3:c.3852+1749_3852+1754delinsACATCC | XP_011537059.1:n.3852+1749_3852+1754delin... | |
| XM_011538758.3:c.3852+1749_3852+1754delinsACATCC | XP_011537060.1:n.3852+1749_3852+1754delin... | |
| XM_011538759.2:c.3852+1749_3852+1754delinsACATCC | XP_011537061.1:n.3852+1749_3852+1754delin... | |
| XM_011538760.2:c.3852+1749_3852+1754delinsACATCC | XP_011537062.1:n.3852+1749_3852+1754delin... | |
| XM_011538761.2:c.3852+1749_3852+1754delinsACATCC | XP_011537063.1:n.3852+1749_3852+1754delin... | |
| XM_011538762.3:c.3084+1749_3084+1754delinsACATCC | XP_011537064.1:n.3084+1749_3084+1754delin... | |
| XM_011538763.3:c.2991+1749_2991+1754delinsACATCC | XP_011537065.1:n.2991+1749_2991+1754delin... | |
| XM_011538764.3:c.3852+1749_3852+1754delinsACATCC | XP_011537066.1:n.3852+1749_3852+1754delin... | |
| XM_011538765.3:c.3852+1749_3852+1754delinsACATCC | XP_011537067.1:n.3852+1749_3852+1754delin... | |
| XM_011538766.3:c.2313+1749_2313+1754delinsACATCC | XP_011537068.1:n.2313+1749_2313+1754delin... | |
| XM_017019980.2:c.3852+1749_3852+1754delinsACATCC | XP_016875469.1:n.3852+1749_3852+1754delin... | |
| XM_017019981.2:c.3852+1749_3852+1754delinsACATCC | XP_016875470.1:n.3852+1749_3852+1754delin... | |
| XM_017019982.1:c.3852+1749_3852+1754delinsACATCC | XP_016875471.1:n.3852+1749_3852+1754delin... | |
| XM_017019983.2:c.2970+1749_2970+1754delinsACATCC | XP_016875472.1:n.2970+1749_2970+1754delin... | |
| XR_001748869.1:n.4196+1749_4196+1754delinsACATCC | ||
| XR_001748870.2:n.4196+1749_4196+1754delinsACATCC | ||
| NM_025114.4:c.2991+1749_2991+1754delinsACATCC MANE Select | NP_079390.3:n.2991+1749_2991+1754delinsAC... |