Linked Data
dbSNP Id:
rs761818188
ExAC:
3:12574248 CCAA / C
gnomAD v2:
3-12574248-CCAA-C
gnomAD v3:
3-12532749-CCAA-C
gnomAD v4:
3-12532749-CCAA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12532754_12532756del , CM000665.2:g.12532754_12532756del | GRCh38 |
| NC_000003.11:g.12574253_12574255del , CM000665.1:g.12574253_12574255del | GRCh37 |
| NC_000003.10:g.12549253_12549255del | NCBI36 |
| NG_011521.1:g.53323_53325del | |
| NG_011521.2:g.53323_53325del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284995.11:c.*33_*35del (TSEN2) MANE Select | ENSP00000284995.6:n.*33_*35del | |
| ENST00000412698.3:c.1260+1095_1260+1097del (TSEN2) | ENSP00000408528.3:n.1260+1095_1260+1097del | |
| ENST00000415684.6:c.*33_*35del (TSEN2) | ENSP00000416510.1:n.*33_*35del | |
| ENST00000444864.6:c.1260+1095_1260+1097del (TSEN2) | ENSP00000407974.2:n.1260+1095_1260+1097del | |
| ENST00000446004.6:c.1338+1095_1338+1097del (TSEN2) | ENSP00000406238.2:n.1338+1095_1338+1097del | |
| ENST00000455118.6:c.*272_*274del (TSEN2) | ENSP00000408744.2:n.*272_*274del | |
| ENST00000475595.2:n.4114_4116del (TSEN2) | ||
| ENST00000679367.1:c.*1050_*1052del (TSEN2) | ENSP00000506510.1:n.*1050_*1052del | |
| ENST00000679420.1:n.1604_1606del (TSEN2) | ||
| ENST00000679424.1:c.*1274_*1276del (TSEN2) | ENSP00000505917.1:n.*1274_*1276del | |
| ENST00000679425.1:c.*33_*35del (TSEN2) | ENSP00000505890.1:n.*33_*35del | |
| ENST00000679492.1:c.1338+1095_1338+1097del (TSEN2) | ENSP00000505331.1:n.1338+1095_1338+1097del | |
| ENST00000679555.1:c.*1154_*1156del (TSEN2) | ENSP00000505538.1:n.*1154_*1156del | |
| ENST00000679670.1:c.*33_*35del (TSEN2) | ENSP00000506080.1:n.*33_*35del | |
| ENST00000679690.1:c.*430_*432del (TSEN2) | ENSP00000506383.1:n.*430_*432del | |
| ENST00000679693.1:c.*175+1095_*175+1097del (TSEN2) | ENSP00000505108.1:n.*175+1095_*175+1097del | |
| ENST00000679699.1:c.*33_*35del (TSEN2) | ENSP00000505274.1:n.*33_*35del | |
| ENST00000679756.1:c.*33_*35del (TSEN2) | ENSP00000506391.1:n.*33_*35del | |
| ENST00000679785.1:c.*272_*274del (TSEN2) | ENSP00000506473.1:n.*272_*274del | |
| ENST00000679835.1:c.*620_*622del (TSEN2) | ENSP00000505616.1:n.*620_*622del | |
| ENST00000679876.1:c.1209+1095_1209+1097del (TSEN2) | ENSP00000504930.1:n.1209+1095_1209+1097del | |
| ENST00000679995.1:c.*272_*274del (TSEN2) | ENSP00000505221.1:n.*272_*274del | |
| ENST00000680126.1:c.*1270_*1272del (TSEN2) | ENSP00000505345.1:n.*1270_*1272del | |
| ENST00000680264.1:c.*527+1095_*527+1097del (TSEN2) | ENSP00000505273.1:n.*527+1095_*527+1097del | |
| ENST00000680275.1:c.*33_*35del (TSEN2) | ENSP00000505417.1:n.*33_*35del | |
| ENST00000680354.1:c.1410_1412del (TSEN2) | ENSP00000505106.1:n.1410_1412del | |
| ENST00000680376.1:c.*620_*622del (TSEN2) | ENSP00000506369.1:n.*620_*622del | |
| ENST00000680421.1:c.*33_*35del (TSEN2) | ENSP00000505530.1:n.*33_*35del | |
| ENST00000680449.1:c.*573_*575del (TSEN2) | ENSP00000505709.1:n.*573_*575del | |
| ENST00000680458.1:c.*246_*248del (TSEN2) | ENSP00000505979.1:n.*246_*248del | |
| ENST00000680555.1:c.*272_*274del (TSEN2) | ENSP00000505160.1:n.*272_*274del | |
| ENST00000680598.1:c.*33_*35del (TSEN2) | ENSP00000506297.1:n.*33_*35del | |
| ENST00000680765.1:c.*272_*274del (TSEN2) | ENSP00000505351.1:n.*272_*274del | |
| ENST00000680817.1:c.*33_*35del (TSEN2) | ENSP00000506221.1:n.*33_*35del | |
| ENST00000680857.1:c.1338+1095_1338+1097del (TSEN2) | ENSP00000506578.1:n.1338+1095_1338+1097del | |
| ENST00000680873.1:c.*583_*585del (TSEN2) | ENSP00000505233.1:n.*583_*585del | |
| ENST00000680923.1:c.*620_*622del (TSEN2) | ENSP00000505344.1:n.*620_*622del | |
| ENST00000680943.1:c.*33_*35del (TSEN2) | ENSP00000505442.1:n.*33_*35del | |
| ENST00000680986.1:c.*33_*35del (TSEN2) | ENSP00000505799.1:n.*33_*35del | |
| ENST00000681042.1:c.1100-6407_1100-6405del (TSEN2) | ENSP00000505622.1:n.1100-6407_1100-6405del | |
| ENST00000681073.1:c.*272_*274del (TSEN2) | ENSP00000506576.1:n.*272_*274del | |
| ENST00000681140.1:c.*33_*35del (TSEN2) | ENSP00000505099.1:n.*33_*35del | |
| ENST00000681227.1:c.*303_*305del (TSEN2) | ENSP00000505240.1:n.*303_*305del | |
| ENST00000681268.1:c.*1575_*1577del (TSEN2) | ENSP00000505385.1:n.*1575_*1577del | |
| ENST00000681343.1:c.*1050_*1052del (TSEN2) | ENSP00000506265.1:n.*1050_*1052del | |
| ENST00000681433.1:c.*272_*274del (TSEN2) | ENSP00000505729.1:n.*272_*274del | |
| ENST00000681471.1:c.*33_*35del (TSEN2) | ENSP00000505105.1:n.*33_*35del | |
| ENST00000681482.1:c.*33_*35del (TSEN2) | ENSP00000505436.1:n.*33_*35del | |
| ENST00000681676.1:c.*33_*35del (TSEN2) | ENSP00000506163.1:n.*33_*35del | |
| ENST00000681713.1:c.*1050_*1052del (TSEN2) | ENSP00000506046.1:n.*1050_*1052del | |
| ENST00000284995.10:c.*33_*35del (TSEN2) | ENSP00000284995.6:n.*33_*35del | |
| ENST00000402228.7:c.*33_*35del (TSEN2) | ENSP00000385976.3:n.*33_*35del | |
| ENST00000412698.2:c.93+1095_93+1097del (TSEN2) | ENSP00000408528.2:n.93+1095_93+1097del | |
| ENST00000415684.5:c.*33_*35del (TSEN2) | ENSP00000416510.1:n.*33_*35del | |
| ENST00000454502.6:c.*33_*35del (TSEN2) | ENSP00000392029.2:n.*33_*35del | |
| ENST00000455118.5:c.278_280del (TSEN2) | ||
| ENST00000473755.5:n.3436_3438del (TSEN2) | ||
| ENST00000475595.1:n.277_279del (TSEN2) | ||
| ENST00000567514.1:n.715+6755_715+6757del (MKRN2OS) | ||
| NM_001145392.1:c.*33_*35del (TSEN2) | NP_001138864.1:n.*33_*35del | |
| NM_001145393.1:c.*33_*35del (TSEN2) | NP_001138865.1:n.*33_*35del | |
| NM_001145394.1:c.*33_*35del (TSEN2) | NP_001138866.1:n.*33_*35del | |
| NM_025265.3:c.*33_*35del (TSEN2) | NP_079541.1:n.*33_*35del | |
| XM_005265495.1:c.*33_*35del (TSEN2) | XP_005265552.1:n.*33_*35del | |
| XM_005265497.1:c.*33_*35del (TSEN2) | XP_005265554.1:n.*33_*35del | |
| XM_005265498.1:c.*33_*35del (TSEN2) | XP_005265555.1:n.*33_*35del | |
| XM_011534138.1:c.*33_*35del (TSEN2) | XP_011532440.1:n.*33_*35del | |
| XM_011534139.1:c.*33_*35del (TSEN2) | XP_011532441.1:n.*33_*35del | |
| XR_245158.1:n.1534_1536del (TSEN2) | ||
| XR_245159.3:n.1534_1536del (TSEN2) | ||
| XR_427295.2:n.3436_3438del (TSEN2) | ||
| XR_427296.1:n.1344_1346del (TSEN2) | ||
| NM_001145393.2:c.*33_*35del (TSEN2) | NP_001138865.1:n.*33_*35del | |
| NM_001321277.1:c.*33_*35del (TSEN2) | NP_001308206.1:n.*33_*35del | |
| NM_001321278.1:c.1338+1095_1338+1097del (TSEN2) | NP_001308207.1:n.1338+1095_1338+1097del | |
| NM_001321279.1:c.*33_*35del (TSEN2) | NP_001308208.1:n.*33_*35del | |
| NR_135607.1:n.1534_1536del (TSEN2) | ||
| XM_011534139.3:c.*33_*35del (TSEN2) | XP_011532441.1:n.*33_*35del | |
| XM_017007292.1:c.*33_*35del (TSEN2) | XP_016862781.1:n.*33_*35del | |
| XM_017007293.1:c.*33_*35del (TSEN2) | XP_016862782.1:n.*33_*35del | |
| XM_017007294.1:c.*33_*35del (TSEN2) | XP_016862783.1:n.*33_*35del | |
| XM_017007295.2:c.*33_*35del (TSEN2) | XP_016862784.1:n.*33_*35del | |
| XM_017007296.2:c.*33_*35del (TSEN2) | XP_016862785.1:n.*33_*35del | |
| XM_017007297.1:c.*33_*35del (TSEN2) | XP_016862786.1:n.*33_*35del | |
| XM_024453785.1:c.*33_*35del (TSEN2) | XP_024309553.1:n.*33_*35del | |
| XR_001740287.1:n.1875_1877del (TSEN2) | ||
| XR_001740288.2:n.1875_1877del (TSEN2) | ||
| XR_001740289.2:n.1818_1820del (TSEN2) | ||
| XR_001740290.2:n.1432_1434del (TSEN2) | ||
| XR_001740291.1:n.1740_1742del (TSEN2) | ||
| XR_001740292.1:n.1838_1840del (TSEN2) | ||
| XR_001740293.1:n.1838_1840del (TSEN2) | ||
| XR_001740294.2:n.1473_1475del (TSEN2) | ||
| XR_001740295.2:n.1395_1397del (TSEN2) | ||
| XR_001740296.1:n.1685_1687del (TSEN2) | ||
| XR_001740297.1:n.2003_2005del (TSEN2) | ||
| XR_001740298.2:n.1320_1322del (TSEN2) | ||
| XR_001740300.2:n.1638_1640del (TSEN2) | ||
| XR_001740301.2:n.1638_1640del (TSEN2) | ||
| XR_001740302.2:n.1601_1603del (TSEN2) | ||
| XR_001740303.2:n.1448_1450del (TSEN2) | ||
| XR_001740304.1:n.1756_1758del (TSEN2) | ||
| XR_002959592.1:n.1609_1611del (TSEN2) | ||
| XR_002959593.1:n.1566_1568del (TSEN2) | ||
| XR_002959594.1:n.1606_1608del (TSEN2) | ||
| XR_002959595.1:n.1946_1948del (TSEN2) | ||
| XR_427296.2:n.1320_1322del (TSEN2) | ||
| NM_001321278.2:c.1338+1095_1338+1097del (TSEN2) | NP_001308207.1:n.1338+1095_1338+1097del | |
| NM_025265.4:c.*33_*35del (TSEN2) MANE Select | NP_079541.1:n.*33_*35del | |
| NR_135607.2:n.1486_1488del (TSEN2) | ||
| NM_001145392.2:c.*33_*35del (TSEN2) | NP_001138864.1:n.*33_*35del | |
| NM_001145393.3:c.*33_*35del (TSEN2) | NP_001138865.1:n.*33_*35del | |
| NM_001145394.2:c.*33_*35del (TSEN2) | NP_001138866.1:n.*33_*35del | |
| NM_001321277.2:c.*33_*35del (TSEN2) | NP_001308206.1:n.*33_*35del | |
| NM_001321279.2:c.*33_*35del (TSEN2) | NP_001308208.1:n.*33_*35del |