Canonical Allele Identifier: CA1346196717

Gene: TSEN2 MKRN2OS

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12532689T= , CM000665.2:g.12532689T=	GRCh38
NC_000003.11:g.12574188T= , CM000665.1:g.12574188T=	GRCh37
NC_000003.10:g.12549188T=	NCBI36
NG_011521.1:g.53258T=
NG_011521.2:g.53258T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284995.11:c.1366T= (TSEN2) MANE Select	ENSP00000284995.6:p.Ser456=
ENST00000412698.3:c.1260+1030T= (TSEN2)	ENSP00000408528.3:n.1260+1030T=
ENST00000415684.6:c.1288T= (TSEN2)	ENSP00000416510.1:p.Ser430=
ENST00000444864.6:c.1260+1030T= (TSEN2)	ENSP00000407974.2:n.1260+1030T=
ENST00000446004.6:c.1338+1030T= (TSEN2)	ENSP00000406238.2:n.1338+1030T=
ENST00000455118.6:c.*207T= (TSEN2)	ENSP00000408744.2:n.*207T=
ENST00000475595.2:n.4049T= (TSEN2)
ENST00000679367.1:c.*985T= (TSEN2)	ENSP00000506510.1:n.*985T=
ENST00000679420.1:n.1539T= (TSEN2)
ENST00000679424.1:c.*1209T= (TSEN2)	ENSP00000505917.1:n.*1209T=
ENST00000679425.1:c.1366T= (TSEN2)	ENSP00000505890.1:p.Ser456=
ENST00000679492.1:c.1338+1030T= (TSEN2)	ENSP00000505331.1:n.1338+1030T=
ENST00000679555.1:c.*1089T= (TSEN2)	ENSP00000505538.1:n.*1089T=
ENST00000679670.1:c.1288T= (TSEN2)	ENSP00000506080.1:p.Ser430=
ENST00000679690.1:c.*365T= (TSEN2)	ENSP00000506383.1:n.*365T=
ENST00000679693.1:c.*175+1030T= (TSEN2)	ENSP00000505108.1:n.*175+1030T=
ENST00000679699.1:c.1366T= (TSEN2)	ENSP00000505274.1:p.Ser456=
ENST00000679756.1:c.1315T= (TSEN2)	ENSP00000506391.1:p.Ser439=
ENST00000679785.1:c.*207T= (TSEN2)	ENSP00000506473.1:n.*207T=
ENST00000679835.1:c.*555T= (TSEN2)	ENSP00000505616.1:n.*555T=
ENST00000679876.1:c.1209+1030T= (TSEN2)	ENSP00000504930.1:n.1209+1030T=
ENST00000679995.1:c.*207T= (TSEN2)	ENSP00000505221.1:n.*207T=
ENST00000680126.1:c.*1205T= (TSEN2)	ENSP00000505345.1:n.*1205T=
ENST00000680264.1:c.*527+1030T= (TSEN2)	ENSP00000505273.1:n.*527+1030T=
ENST00000680275.1:c.1423T= (TSEN2)	ENSP00000505417.1:p.Ser475=
ENST00000680354.1:c.1345T= (TSEN2)	ENSP00000505106.1:p.Ser449=
ENST00000680376.1:c.*555T= (TSEN2)	ENSP00000506369.1:n.*555T=
ENST00000680421.1:c.1237T= (TSEN2)	ENSP00000505530.1:p.Ser413=
ENST00000680449.1:c.*508T= (TSEN2)	ENSP00000505709.1:n.*508T=
ENST00000680458.1:c.*181T= (TSEN2)	ENSP00000505979.1:n.*181T=
ENST00000680555.1:c.*207T= (TSEN2)	ENSP00000505160.1:n.*207T=
ENST00000680598.1:c.1315T= (TSEN2)	ENSP00000506297.1:p.Ser439=
ENST00000680765.1:c.*207T= (TSEN2)	ENSP00000505351.1:n.*207T=
ENST00000680817.1:c.1237T= (TSEN2)	ENSP00000506221.1:p.Ser413=
ENST00000680857.1:c.1338+1030T= (TSEN2)	ENSP00000506578.1:n.1338+1030T=
ENST00000680873.1:c.*518T= (TSEN2)	ENSP00000505233.1:n.*518T=
ENST00000680923.1:c.*555T= (TSEN2)	ENSP00000505344.1:n.*555T=
ENST00000680943.1:c.1315T= (TSEN2)	ENSP00000505442.1:p.Ser439=
ENST00000680986.1:c.1366T= (TSEN2)	ENSP00000505799.1:p.Ser456=
ENST00000681042.1:c.1100-6472T= (TSEN2)	ENSP00000505622.1:n.1100-6472T=
ENST00000681073.1:c.*207T= (TSEN2)	ENSP00000506576.1:n.*207T=
ENST00000681140.1:c.1366T= (TSEN2)	ENSP00000505099.1:p.Ser456=
ENST00000681227.1:c.*238T= (TSEN2)	ENSP00000505240.1:n.*238T=
ENST00000681268.1:c.*1510T= (TSEN2)	ENSP00000505385.1:n.*1510T=
ENST00000681343.1:c.*985T= (TSEN2)	ENSP00000506265.1:n.*985T=
ENST00000681433.1:c.*207T= (TSEN2)	ENSP00000505729.1:n.*207T=
ENST00000681471.1:c.1288T= (TSEN2)	ENSP00000505105.1:p.Ser430=
ENST00000681482.1:c.1366T= (TSEN2)	ENSP00000505436.1:p.Ser456=
ENST00000681676.1:c.1288T= (TSEN2)	ENSP00000506163.1:p.Ser430=
ENST00000681713.1:c.*985T= (TSEN2)	ENSP00000506046.1:n.*985T=
ENST00000284995.10:c.1366T= (TSEN2)	ENSP00000284995.6:p.Ser456=
ENST00000402228.7:c.1366T= (TSEN2)	ENSP00000385976.3:p.Ser456=
ENST00000412698.2:c.93+1030T= (TSEN2)	ENSP00000408528.2:n.93+1030T=
ENST00000415684.5:c.1288T= (TSEN2)	ENSP00000416510.1:p.Ser430=
ENST00000454502.6:c.1189T= (TSEN2)	ENSP00000392029.2:p.Ser397=
ENST00000455118.5:c.213T= (TSEN2)
ENST00000473755.5:n.3371T= (TSEN2)
ENST00000475595.1:n.212T= (TSEN2)
ENST00000567514.1:n.715+6818A= (MKRN2OS)
NM_001145392.1:c.1366T= (TSEN2)	NP_001138864.1:p.Ser456=
NM_001145393.1:c.1288T= (TSEN2)	NP_001138865.1:p.Ser430=
NM_001145394.1:c.1189T= (TSEN2)	NP_001138866.1:p.Ser397=
NM_025265.3:c.1366T= (TSEN2)	NP_079541.1:p.Ser456=
XM_005265495.1:c.1366T= (TSEN2)	XP_005265552.1:p.Ser456=
XM_005265497.1:c.1288T= (TSEN2)	XP_005265554.1:p.Ser430=
XM_005265498.1:c.1237T= (TSEN2)	XP_005265555.1:p.Ser413=
XM_011534138.1:c.1099T= (TSEN2)	XP_011532440.1:p.Ser367=
XM_011534139.1:c.1093T= (TSEN2)	XP_011532441.1:p.Ser365=
XR_245158.1:n.1469T= (TSEN2)
XR_245159.3:n.1469T= (TSEN2)
XR_427295.2:n.3371T= (TSEN2)
XR_427296.1:n.1279T= (TSEN2)
NM_001145393.2:c.1288T= (TSEN2)	NP_001138865.1:p.Ser430=
NM_001321277.1:c.1366T= (TSEN2)	NP_001308206.1:p.Ser456=
NM_001321278.1:c.1338+1030T= (TSEN2)	NP_001308207.1:n.1338+1030T=
NM_001321279.1:c.1288T= (TSEN2)	NP_001308208.1:p.Ser430=
NR_135607.1:n.1469T= (TSEN2)
XM_011534139.3:c.1093T= (TSEN2)	XP_011532441.1:p.Ser365=
XM_017007292.1:c.1423T= (TSEN2)	XP_016862781.1:p.Ser475=
XM_017007293.1:c.1423T= (TSEN2)	XP_016862782.1:p.Ser475=
XM_017007294.1:c.1423T= (TSEN2)	XP_016862783.1:p.Ser475=
XM_017007295.2:c.1423T= (TSEN2)	XP_016862784.1:p.Ser475=
XM_017007296.2:c.1366T= (TSEN2)	XP_016862785.1:p.Ser456=
XM_017007297.1:c.1345T= (TSEN2)	XP_016862786.1:p.Ser449=
XM_024453785.1:c.1288T= (TSEN2)	XP_024309553.1:p.Ser430=
XR_001740287.1:n.1810T= (TSEN2)
XR_001740288.2:n.1810T= (TSEN2)
XR_001740289.2:n.1753T= (TSEN2)
XR_001740290.2:n.1367T= (TSEN2)
XR_001740291.1:n.1675T= (TSEN2)
XR_001740292.1:n.1773T= (TSEN2)
XR_001740293.1:n.1773T= (TSEN2)
XR_001740294.2:n.1408T= (TSEN2)
XR_001740295.2:n.1330T= (TSEN2)
XR_001740296.1:n.1620T= (TSEN2)
XR_001740297.1:n.1938T= (TSEN2)
XR_001740298.2:n.1255T= (TSEN2)
XR_001740300.2:n.1573T= (TSEN2)
XR_001740301.2:n.1573T= (TSEN2)
XR_001740302.2:n.1536T= (TSEN2)
XR_001740303.2:n.1383T= (TSEN2)
XR_001740304.1:n.1691T= (TSEN2)
XR_002959592.1:n.1544T= (TSEN2)
XR_002959593.1:n.1501T= (TSEN2)
XR_002959594.1:n.1541T= (TSEN2)
XR_002959595.1:n.1881T= (TSEN2)
XR_427296.2:n.1255T= (TSEN2)
NM_001321278.2:c.1338+1030T= (TSEN2)	NP_001308207.1:n.1338+1030T=
NM_025265.4:c.1366T= (TSEN2) MANE Select	NP_079541.1:p.Ser456=
NR_135607.2:n.1421T= (TSEN2)
NM_001145392.2:c.1366T= (TSEN2)	NP_001138864.1:p.Ser456=
NM_001145393.3:c.1288T= (TSEN2)	NP_001138865.1:p.Ser430=
NM_001145394.2:c.1189T= (TSEN2)	NP_001138866.1:p.Ser397=
NM_001321277.2:c.1366T= (TSEN2)	NP_001308206.1:p.Ser456=
NM_001321279.2:c.1288T= (TSEN2)	NP_001308208.1:p.Ser430=