ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.88115145_88115146del , CM000674.2:g.88115145_88115146del | GRCh38 |
| NC_000012.11:g.88508922_88508923del , CM000674.1:g.88508922_88508923del | GRCh37 |
| NC_000012.10:g.87033053_87033054del | NCBI36 |
| NG_008417.1:g.32074_32075del | |
| NG_008417.2:g.32074_32075del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309041.12:c.1864_1865del | ENSP00000308021.8:p.Asp622PhefsTer5 | |
| ENST00000547926.7:c.1864_1865del | ENSP00000448573.3:p.Asp622PhefsTer5 | |
| ENST00000552810.6:c.1864_1865del MANE Select | ENSP00000448012.1:p.Asp622PhefsTer5 | |
| ENST00000671822.2:n.3420_3421del | ||
| ENST00000672414.2:c.*35_*36del | ENSP00000500729.1:n.*35_*36del | |
| ENST00000673058.2:c.1864_1865del | ENSP00000500665.2:p.Asp622PhefsTer5 | |
| ENST00000674971.1:c.1864_1865del | ENSP00000502194.1:p.Asp622PhefsTer5 | |
| ENST00000675230.1:c.1843_1844del | ENSP00000502503.1:p.Asp615PhefsTer5 | |
| ENST00000675408.1:c.1864_1865del | ENSP00000502298.1:p.Asp622PhefsTer5 | |
| ENST00000675476.1:c.2725_2726del | ENSP00000502161.1:p.Asp909PhefsTer5 | |
| ENST00000675628.1:n.2091_2092del | ||
| ENST00000675794.1:c.*35_*36del | ENSP00000502841.1:n.*35_*36del | |
| ENST00000675833.1:c.2632_2633del | ENSP00000502559.1:p.Asp878PhefsTer5 | |
| ENST00000676074.1:c.1864_1865del | ENSP00000502079.1:p.Asp622PhefsTer5 | |
| ENST00000676351.1:c.*2819_*2820del | ENSP00000502046.1:n.*2819_*2820del | |
| ENST00000676363.1:n.3927_3928del | ||
| ENST00000676448.1:c.1864_1865del | ENSP00000501987.1:p.Asp622PhefsTer5 | |
| ENST00000309041.11:c.1870_1871del | ENSP00000308021.7:p.Asp624PhefsTer5 | |
| ENST00000397838.7:c.1870_1871del | ENSP00000380938.4:p.Asp624PhefsTer5 | |
| ENST00000547926.6:c.1762_1763del | ENSP00000448573.2:p.Asp588PhefsTer5 | |
| ENST00000552810.5:c.1864_1865del | ENSP00000448012.1:p.Asp622PhefsTer5 | |
| ENST00000604024.5:c.1123_1124del | ENSP00000473863.1:p.Asp375PhefsTer5 | |
| NM_025114.3:c.1864_1865del | NP_079390.3:p.Asp622PhefsTer5 | |
| XM_011538756.1:c.2725_2726del | XP_011537058.1:p.Asp909PhefsTer5 | |
| XM_011538757.1:c.2725_2726del | XP_011537059.1:p.Asp909PhefsTer5 | |
| XM_011538758.1:c.2725_2726del | XP_011537060.1:p.Asp909PhefsTer5 | |
| XM_011538759.1:c.2725_2726del | XP_011537061.1:p.Asp909PhefsTer5 | |
| XM_011538760.1:c.2725_2726del | XP_011537062.1:p.Asp909PhefsTer5 | |
| XM_011538761.1:c.2725_2726del | XP_011537063.1:p.Asp909PhefsTer5 | |
| XM_011538762.1:c.1957_1958del | XP_011537064.1:p.Asp653PhefsTer5 | |
| XM_011538763.1:c.1864_1865del | XP_011537065.1:p.Asp622PhefsTer5 | |
| XM_011538764.1:c.2725_2726del | XP_011537066.1:p.Asp909PhefsTer5 | |
| XM_011538765.1:c.2725_2726del | XP_011537067.1:p.Asp909PhefsTer5 | |
| XM_011538766.1:c.1186_1187del | XP_011537068.1:p.Asp396PhefsTer5 | |
| XM_011538756.3:c.2725_2726del | XP_011537058.1:p.Asp909PhefsTer5 | |
| XM_011538757.3:c.2725_2726del | XP_011537059.1:p.Asp909PhefsTer5 | |
| XM_011538758.3:c.2725_2726del | XP_011537060.1:p.Asp909PhefsTer5 | |
| XM_011538759.2:c.2725_2726del | XP_011537061.1:p.Asp909PhefsTer5 | |
| XM_011538760.2:c.2725_2726del | XP_011537062.1:p.Asp909PhefsTer5 | |
| XM_011538761.2:c.2725_2726del | XP_011537063.1:p.Asp909PhefsTer5 | |
| XM_011538762.3:c.1957_1958del | XP_011537064.1:p.Asp653PhefsTer5 | |
| XM_011538763.3:c.1864_1865del | XP_011537065.1:p.Asp622PhefsTer5 | |
| XM_011538764.3:c.2725_2726del | XP_011537066.1:p.Asp909PhefsTer5 | |
| XM_011538765.3:c.2725_2726del | XP_011537067.1:p.Asp909PhefsTer5 | |
| XM_011538766.3:c.1186_1187del | XP_011537068.1:p.Asp396PhefsTer5 | |
| XM_017019980.2:c.2725_2726del | XP_016875469.1:p.Asp909PhefsTer5 | |
| XM_017019981.2:c.2725_2726del | XP_016875470.1:p.Asp909PhefsTer5 | |
| XM_017019982.1:c.2725_2726del | XP_016875471.1:p.Asp909PhefsTer5 | |
| XM_017019983.2:c.1843_1844del | XP_016875472.1:p.Asp615PhefsTer5 | |
| XR_001748869.1:n.3069_3070del | ||
| XR_001748870.2:n.3069_3070del | ||
| NM_025114.4:c.1864_1865del MANE Select | NP_079390.3:p.Asp622PhefsTer5 |