Canonical Allele Identifier: CA351478459
Gene: TSEN2 HGNC NCBI
MKRN2OS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12532690C>A , CM000665.2:g.12532690C>A GRCh38
NC_000003.11:g.12574189C>A , CM000665.1:g.12574189C>A GRCh37
NC_000003.10:g.12549189C>A NCBI36
NG_011521.1:g.53259C>A
NG_011521.2:g.53259C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000284995.11:c.1367C>A (TSEN2) MANE Select ENSP00000284995.6:p.Ser456Ter
ENST00000412698.3:c.1260+1031C>A (TSEN2) ENSP00000408528.3:n.1260+1031C>A
ENST00000415684.6:c.1289C>A (TSEN2) ENSP00000416510.1:p.Ser430Ter
ENST00000444864.6:c.1260+1031C>A (TSEN2) ENSP00000407974.2:n.1260+1031C>A
ENST00000446004.6:c.1338+1031C>A (TSEN2) ENSP00000406238.2:n.1338+1031C>A
ENST00000455118.6:c.*208C>A (TSEN2) ENSP00000408744.2:n.*208C>A
ENST00000475595.2:n.4050C>A (TSEN2)
ENST00000679367.1:c.*986C>A (TSEN2) ENSP00000506510.1:n.*986C>A
ENST00000679420.1:n.1540C>A (TSEN2)
ENST00000679424.1:c.*1210C>A (TSEN2) ENSP00000505917.1:n.*1210C>A
ENST00000679425.1:c.1367C>A (TSEN2) ENSP00000505890.1:p.Ser456Ter
ENST00000679492.1:c.1338+1031C>A (TSEN2) ENSP00000505331.1:n.1338+1031C>A
ENST00000679555.1:c.*1090C>A (TSEN2) ENSP00000505538.1:n.*1090C>A
ENST00000679670.1:c.1289C>A (TSEN2) ENSP00000506080.1:p.Ser430Ter
ENST00000679690.1:c.*366C>A (TSEN2) ENSP00000506383.1:n.*366C>A
ENST00000679693.1:c.*175+1031C>A (TSEN2) ENSP00000505108.1:n.*175+1031C>A
ENST00000679699.1:c.1367C>A (TSEN2) ENSP00000505274.1:p.Ser456Ter
ENST00000679756.1:c.1316C>A (TSEN2) ENSP00000506391.1:p.Ser439Ter
ENST00000679785.1:c.*208C>A (TSEN2) ENSP00000506473.1:n.*208C>A
ENST00000679835.1:c.*556C>A (TSEN2) ENSP00000505616.1:n.*556C>A
ENST00000679876.1:c.1209+1031C>A (TSEN2) ENSP00000504930.1:n.1209+1031C>A
ENST00000679995.1:c.*208C>A (TSEN2) ENSP00000505221.1:n.*208C>A
ENST00000680126.1:c.*1206C>A (TSEN2) ENSP00000505345.1:n.*1206C>A
ENST00000680264.1:c.*527+1031C>A (TSEN2) ENSP00000505273.1:n.*527+1031C>A
ENST00000680275.1:c.1424C>A (TSEN2) ENSP00000505417.1:p.Ser475Ter
ENST00000680354.1:c.1346C>A (TSEN2) ENSP00000505106.1:p.Ser449Ter
ENST00000680376.1:c.*556C>A (TSEN2) ENSP00000506369.1:n.*556C>A
ENST00000680421.1:c.1238C>A (TSEN2) ENSP00000505530.1:p.Ser413Ter
ENST00000680449.1:c.*509C>A (TSEN2) ENSP00000505709.1:n.*509C>A
ENST00000680458.1:c.*182C>A (TSEN2) ENSP00000505979.1:n.*182C>A
ENST00000680555.1:c.*208C>A (TSEN2) ENSP00000505160.1:n.*208C>A
ENST00000680598.1:c.1316C>A (TSEN2) ENSP00000506297.1:p.Ser439Ter
ENST00000680765.1:c.*208C>A (TSEN2) ENSP00000505351.1:n.*208C>A
ENST00000680817.1:c.1238C>A (TSEN2) ENSP00000506221.1:p.Ser413Ter
ENST00000680857.1:c.1338+1031C>A (TSEN2) ENSP00000506578.1:n.1338+1031C>A
ENST00000680873.1:c.*519C>A (TSEN2) ENSP00000505233.1:n.*519C>A
ENST00000680923.1:c.*556C>A (TSEN2) ENSP00000505344.1:n.*556C>A
ENST00000680943.1:c.1316C>A (TSEN2) ENSP00000505442.1:p.Ser439Ter
ENST00000680986.1:c.1367C>A (TSEN2) ENSP00000505799.1:p.Ser456Ter
ENST00000681042.1:c.1100-6471C>A (TSEN2) ENSP00000505622.1:n.1100-6471C>A
ENST00000681073.1:c.*208C>A (TSEN2) ENSP00000506576.1:n.*208C>A
ENST00000681140.1:c.1367C>A (TSEN2) ENSP00000505099.1:p.Ser456Ter
ENST00000681227.1:c.*239C>A (TSEN2) ENSP00000505240.1:n.*239C>A
ENST00000681268.1:c.*1511C>A (TSEN2) ENSP00000505385.1:n.*1511C>A
ENST00000681343.1:c.*986C>A (TSEN2) ENSP00000506265.1:n.*986C>A
ENST00000681433.1:c.*208C>A (TSEN2) ENSP00000505729.1:n.*208C>A
ENST00000681471.1:c.1289C>A (TSEN2) ENSP00000505105.1:p.Ser430Ter
ENST00000681482.1:c.1367C>A (TSEN2) ENSP00000505436.1:p.Ser456Ter
ENST00000681676.1:c.1289C>A (TSEN2) ENSP00000506163.1:p.Ser430Ter
ENST00000681713.1:c.*986C>A (TSEN2) ENSP00000506046.1:n.*986C>A
ENST00000284995.10:c.1367C>A (TSEN2) ENSP00000284995.6:p.Ser456Ter
ENST00000402228.7:c.1367C>A (TSEN2) ENSP00000385976.3:p.Ser456Ter
ENST00000412698.2:c.93+1031C>A (TSEN2) ENSP00000408528.2:n.93+1031C>A
ENST00000415684.5:c.1289C>A (TSEN2) ENSP00000416510.1:p.Ser430Ter
ENST00000454502.6:c.1190C>A (TSEN2) ENSP00000392029.2:p.Ser397Ter
ENST00000455118.5:c.214C>A (TSEN2)
ENST00000473755.5:n.3372C>A (TSEN2)
ENST00000475595.1:n.213C>A (TSEN2)
ENST00000567514.1:n.715+6817G>T (MKRN2OS)
NM_001145392.1:c.1367C>A (TSEN2) NP_001138864.1:p.Ser456Ter
NM_001145393.1:c.1289C>A (TSEN2) NP_001138865.1:p.Ser430Ter
NM_001145394.1:c.1190C>A (TSEN2) NP_001138866.1:p.Ser397Ter
NM_025265.3:c.1367C>A (TSEN2) NP_079541.1:p.Ser456Ter
XM_005265495.1:c.1367C>A (TSEN2) XP_005265552.1:p.Ser456Ter
XM_005265497.1:c.1289C>A (TSEN2) XP_005265554.1:p.Ser430Ter
XM_005265498.1:c.1238C>A (TSEN2) XP_005265555.1:p.Ser413Ter
XM_011534138.1:c.1100C>A (TSEN2) XP_011532440.1:p.Ser367Ter
XM_011534139.1:c.1094C>A (TSEN2) XP_011532441.1:p.Ser365Ter
XR_245158.1:n.1470C>A (TSEN2)
XR_245159.3:n.1470C>A (TSEN2)
XR_427295.2:n.3372C>A (TSEN2)
XR_427296.1:n.1280C>A (TSEN2)
NM_001145393.2:c.1289C>A (TSEN2) NP_001138865.1:p.Ser430Ter
NM_001321277.1:c.1367C>A (TSEN2) NP_001308206.1:p.Ser456Ter
NM_001321278.1:c.1338+1031C>A (TSEN2) NP_001308207.1:n.1338+1031C>A
NM_001321279.1:c.1289C>A (TSEN2) NP_001308208.1:p.Ser430Ter
NR_135607.1:n.1470C>A (TSEN2)
XM_011534139.3:c.1094C>A (TSEN2) XP_011532441.1:p.Ser365Ter
XM_017007292.1:c.1424C>A (TSEN2) XP_016862781.1:p.Ser475Ter
XM_017007293.1:c.1424C>A (TSEN2) XP_016862782.1:p.Ser475Ter
XM_017007294.1:c.1424C>A (TSEN2) XP_016862783.1:p.Ser475Ter
XM_017007295.2:c.1424C>A (TSEN2) XP_016862784.1:p.Ser475Ter
XM_017007296.2:c.1367C>A (TSEN2) XP_016862785.1:p.Ser456Ter
XM_017007297.1:c.1346C>A (TSEN2) XP_016862786.1:p.Ser449Ter
XM_024453785.1:c.1289C>A (TSEN2) XP_024309553.1:p.Ser430Ter
XR_001740287.1:n.1811C>A (TSEN2)
XR_001740288.2:n.1811C>A (TSEN2)
XR_001740289.2:n.1754C>A (TSEN2)
XR_001740290.2:n.1368C>A (TSEN2)
XR_001740291.1:n.1676C>A (TSEN2)
XR_001740292.1:n.1774C>A (TSEN2)
XR_001740293.1:n.1774C>A (TSEN2)
XR_001740294.2:n.1409C>A (TSEN2)
XR_001740295.2:n.1331C>A (TSEN2)
XR_001740296.1:n.1621C>A (TSEN2)
XR_001740297.1:n.1939C>A (TSEN2)
XR_001740298.2:n.1256C>A (TSEN2)
XR_001740300.2:n.1574C>A (TSEN2)
XR_001740301.2:n.1574C>A (TSEN2)
XR_001740302.2:n.1537C>A (TSEN2)
XR_001740303.2:n.1384C>A (TSEN2)
XR_001740304.1:n.1692C>A (TSEN2)
XR_002959592.1:n.1545C>A (TSEN2)
XR_002959593.1:n.1502C>A (TSEN2)
XR_002959594.1:n.1542C>A (TSEN2)
XR_002959595.1:n.1882C>A (TSEN2)
XR_427296.2:n.1256C>A (TSEN2)
NM_001321278.2:c.1338+1031C>A (TSEN2) NP_001308207.1:n.1338+1031C>A
NM_025265.4:c.1367C>A (TSEN2) MANE Select NP_079541.1:p.Ser456Ter
NR_135607.2:n.1422C>A (TSEN2)
NM_001145392.2:c.1367C>A (TSEN2) NP_001138864.1:p.Ser456Ter
NM_001145393.3:c.1289C>A (TSEN2) NP_001138865.1:p.Ser430Ter
NM_001145394.2:c.1190C>A (TSEN2) NP_001138866.1:p.Ser397Ter
NM_001321277.2:c.1367C>A (TSEN2) NP_001308206.1:p.Ser456Ter
NM_001321279.2:c.1289C>A (TSEN2) NP_001308208.1:p.Ser430Ter