Linked Data
ClinVar Variation Id:
217622
ClinVar RCV Id:
RCV000201771
RCV000697843
RCV001002938
RCV000988888
RCV001075310
RCV001268720
RCV001376373
RCV002500629
RCV003468916
dbSNP Id:
rs727503855
ExAC:
12:88512304 AT / A
gnomAD v2:
12-88512304-AT-A
gnomAD v3:
12-88118527-AT-A
gnomAD v4:
12-88118527-AT-A
PubMed:
PMID:26092869
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.88118537del , CM000674.2:g.88118537del | GRCh38 |
| NC_000012.11:g.88512314del , CM000674.1:g.88512314del | GRCh37 |
| NC_000012.10:g.87036445del | NCBI36 |
| NG_008417.1:g.28689del | |
| NG_008417.2:g.28689del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309041.12:c.1666del | ENSP00000308021.8:p.Ile556PhefsTer17 | |
| ENST00000397838.8:c.1612del | ENSP00000380938.5:p.Ile538PhefsTer17 | |
| ENST00000547926.7:c.1666del | ENSP00000448573.3:p.Ile556PhefsTer17 | |
| ENST00000552810.6:c.1666del MANE Select | ENSP00000448012.1:p.Ile556PhefsTer17 | |
| ENST00000671822.2:n.3335del | ||
| ENST00000672414.2:c.1666del | ENSP00000500729.1:p.Ile556PhefsTer? | |
| ENST00000673058.2:c.1666del | ENSP00000500665.2:p.Ile556PhefsTer17 | |
| ENST00000674971.1:c.1666del | ENSP00000502194.1:p.Ile556PhefsTer17 | |
| ENST00000675230.1:c.1645del | ENSP00000502503.1:p.Ile549PhefsTer17 | |
| ENST00000675408.1:c.1666del | ENSP00000502298.1:p.Ile556PhefsTer17 | |
| ENST00000675476.1:c.1666del | ENSP00000502161.1:p.Ile556PhefsTer17 | |
| ENST00000675559.1:c.*212del | ENSP00000502163.1:n.*212del | |
| ENST00000675628.1:n.1893del | ||
| ENST00000675794.1:c.1666del | ENSP00000502841.1:p.Ile556PhefsTer? | |
| ENST00000675833.1:c.1666del | ENSP00000502559.1:p.Ile556PhefsTer17 | |
| ENST00000676074.1:c.1666del | ENSP00000502079.1:p.Ile556PhefsTer17 | |
| ENST00000676351.1:c.*2621del | ENSP00000502046.1:n.*2621del | |
| ENST00000676363.1:n.3729del | ||
| ENST00000676418.1:c.*123del | ENSP00000502371.1:n.*123del | |
| ENST00000676448.1:c.1666del | ENSP00000501987.1:p.Ile556PhefsTer17 | |
| ENST00000309041.11:c.1672del | ENSP00000308021.7:p.Ile558PhefsTer17 | |
| ENST00000397838.7:c.1672del | ENSP00000380938.4:p.Ile558PhefsTer17 | |
| ENST00000547926.6:c.1564del | ENSP00000448573.2:p.Ile522PhefsTer17 | |
| ENST00000552810.5:c.1666del | ENSP00000448012.1:p.Ile556PhefsTer17 | |
| ENST00000604024.5:c.832del | ENSP00000473863.1:p.Ile278PhefsTer17 | |
| NM_025114.3:c.1666del | NP_079390.3:p.Ile556PhefsTer17 | |
| XM_011538756.1:c.1666del | XP_011537058.1:p.Ile556PhefsTer17 | |
| XM_011538757.1:c.1666del | XP_011537059.1:p.Ile556PhefsTer17 | |
| XM_011538758.1:c.1666del | XP_011537060.1:p.Ile556PhefsTer17 | |
| XM_011538759.1:c.1666del | XP_011537061.1:p.Ile556PhefsTer17 | |
| XM_011538760.1:c.1666del | XP_011537062.1:p.Ile556PhefsTer17 | |
| XM_011538761.1:c.1666del | XP_011537063.1:p.Ile556PhefsTer17 | |
| XM_011538762.1:c.1666del | XP_011537064.1:p.Ile556PhefsTer17 | |
| XM_011538763.1:c.1666del | XP_011537065.1:p.Ile556PhefsTer17 | |
| XM_011538764.1:c.1666del | XP_011537066.1:p.Ile556PhefsTer17 | |
| XM_011538765.1:c.1666del | XP_011537067.1:p.Ile556PhefsTer17 | |
| XM_011538766.1:c.127del | XP_011537068.1:p.Ile43PhefsTer17 | |
| XM_011538756.3:c.1666del | XP_011537058.1:p.Ile556PhefsTer17 | |
| XM_011538757.3:c.1666del | XP_011537059.1:p.Ile556PhefsTer17 | |
| XM_011538758.3:c.1666del | XP_011537060.1:p.Ile556PhefsTer17 | |
| XM_011538759.2:c.1666del | XP_011537061.1:p.Ile556PhefsTer17 | |
| XM_011538760.2:c.1666del | XP_011537062.1:p.Ile556PhefsTer17 | |
| XM_011538761.2:c.1666del | XP_011537063.1:p.Ile556PhefsTer17 | |
| XM_011538762.3:c.1666del | XP_011537064.1:p.Ile556PhefsTer17 | |
| XM_011538763.3:c.1666del | XP_011537065.1:p.Ile556PhefsTer17 | |
| XM_011538764.3:c.1666del | XP_011537066.1:p.Ile556PhefsTer17 | |
| XM_011538765.3:c.1666del | XP_011537067.1:p.Ile556PhefsTer17 | |
| XM_011538766.3:c.127del | XP_011537068.1:p.Ile43PhefsTer17 | |
| XM_017019980.2:c.1666del | XP_016875469.1:p.Ile556PhefsTer17 | |
| XM_017019981.2:c.1666del | XP_016875470.1:p.Ile556PhefsTer17 | |
| XM_017019982.1:c.1666del | XP_016875471.1:p.Ile556PhefsTer17 | |
| XM_017019983.2:c.1645del | XP_016875472.1:p.Ile549PhefsTer17 | |
| XR_001748869.1:n.2010del | ||
| XR_001748870.2:n.2010del | ||
| NM_025114.4:c.1666del MANE Select | NP_079390.3:p.Ile556PhefsTer17 |