Canonical Allele Identifier: CA1346196710

Gene: TSEN2 MKRN2OS

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12532681G= , CM000665.2:g.12532681G=	GRCh38
NC_000003.11:g.12574180G= , CM000665.1:g.12574180G=	GRCh37
NC_000003.10:g.12549180G=	NCBI36
NG_011521.1:g.53250G=
NG_011521.2:g.53250G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284995.11:c.1358G= (TSEN2) MANE Select	ENSP00000284995.6:p.Trp453=
ENST00000412698.3:c.1260+1022G= (TSEN2)	ENSP00000408528.3:n.1260+1022G=
ENST00000415684.6:c.1280G= (TSEN2)	ENSP00000416510.1:p.Trp427=
ENST00000444864.6:c.1260+1022G= (TSEN2)	ENSP00000407974.2:n.1260+1022G=
ENST00000446004.6:c.1338+1022G= (TSEN2)	ENSP00000406238.2:n.1338+1022G=
ENST00000455118.6:c.*199G= (TSEN2)	ENSP00000408744.2:n.*199G=
ENST00000475595.2:n.4041G= (TSEN2)
ENST00000679367.1:c.*977G= (TSEN2)	ENSP00000506510.1:n.*977G=
ENST00000679420.1:n.1531G= (TSEN2)
ENST00000679424.1:c.*1201G= (TSEN2)	ENSP00000505917.1:n.*1201G=
ENST00000679425.1:c.1358G= (TSEN2)	ENSP00000505890.1:p.Trp453=
ENST00000679492.1:c.1338+1022G= (TSEN2)	ENSP00000505331.1:n.1338+1022G=
ENST00000679555.1:c.*1081G= (TSEN2)	ENSP00000505538.1:n.*1081G=
ENST00000679670.1:c.1280G= (TSEN2)	ENSP00000506080.1:p.Trp427=
ENST00000679690.1:c.*357G= (TSEN2)	ENSP00000506383.1:n.*357G=
ENST00000679693.1:c.*175+1022G= (TSEN2)	ENSP00000505108.1:n.*175+1022G=
ENST00000679699.1:c.1358G= (TSEN2)	ENSP00000505274.1:p.Trp453=
ENST00000679756.1:c.1307G= (TSEN2)	ENSP00000506391.1:p.Trp436=
ENST00000679785.1:c.*199G= (TSEN2)	ENSP00000506473.1:n.*199G=
ENST00000679835.1:c.*547G= (TSEN2)	ENSP00000505616.1:n.*547G=
ENST00000679876.1:c.1209+1022G= (TSEN2)	ENSP00000504930.1:n.1209+1022G=
ENST00000679995.1:c.*199G= (TSEN2)	ENSP00000505221.1:n.*199G=
ENST00000680126.1:c.*1197G= (TSEN2)	ENSP00000505345.1:n.*1197G=
ENST00000680264.1:c.*527+1022G= (TSEN2)	ENSP00000505273.1:n.*527+1022G=
ENST00000680275.1:c.1415G= (TSEN2)	ENSP00000505417.1:p.Trp472=
ENST00000680354.1:c.1337G= (TSEN2)	ENSP00000505106.1:p.Trp446=
ENST00000680376.1:c.*547G= (TSEN2)	ENSP00000506369.1:n.*547G=
ENST00000680421.1:c.1229G= (TSEN2)	ENSP00000505530.1:p.Trp410=
ENST00000680449.1:c.*500G= (TSEN2)	ENSP00000505709.1:n.*500G=
ENST00000680458.1:c.*173G= (TSEN2)	ENSP00000505979.1:n.*173G=
ENST00000680555.1:c.*199G= (TSEN2)	ENSP00000505160.1:n.*199G=
ENST00000680598.1:c.1307G= (TSEN2)	ENSP00000506297.1:p.Trp436=
ENST00000680765.1:c.*199G= (TSEN2)	ENSP00000505351.1:n.*199G=
ENST00000680817.1:c.1229G= (TSEN2)	ENSP00000506221.1:p.Trp410=
ENST00000680857.1:c.1338+1022G= (TSEN2)	ENSP00000506578.1:n.1338+1022G=
ENST00000680873.1:c.*510G= (TSEN2)	ENSP00000505233.1:n.*510G=
ENST00000680923.1:c.*547G= (TSEN2)	ENSP00000505344.1:n.*547G=
ENST00000680943.1:c.1307G= (TSEN2)	ENSP00000505442.1:p.Trp436=
ENST00000680986.1:c.1358G= (TSEN2)	ENSP00000505799.1:p.Trp453=
ENST00000681042.1:c.1100-6480G= (TSEN2)	ENSP00000505622.1:n.1100-6480G=
ENST00000681073.1:c.*199G= (TSEN2)	ENSP00000506576.1:n.*199G=
ENST00000681140.1:c.1358G= (TSEN2)	ENSP00000505099.1:p.Trp453=
ENST00000681227.1:c.*230G= (TSEN2)	ENSP00000505240.1:n.*230G=
ENST00000681268.1:c.*1502G= (TSEN2)	ENSP00000505385.1:n.*1502G=
ENST00000681343.1:c.*977G= (TSEN2)	ENSP00000506265.1:n.*977G=
ENST00000681433.1:c.*199G= (TSEN2)	ENSP00000505729.1:n.*199G=
ENST00000681471.1:c.1280G= (TSEN2)	ENSP00000505105.1:p.Trp427=
ENST00000681482.1:c.1358G= (TSEN2)	ENSP00000505436.1:p.Trp453=
ENST00000681676.1:c.1280G= (TSEN2)	ENSP00000506163.1:p.Trp427=
ENST00000681713.1:c.*977G= (TSEN2)	ENSP00000506046.1:n.*977G=
ENST00000284995.10:c.1358G= (TSEN2)	ENSP00000284995.6:p.Trp453=
ENST00000402228.7:c.1358G= (TSEN2)	ENSP00000385976.3:p.Trp453=
ENST00000412698.2:c.93+1022G= (TSEN2)	ENSP00000408528.2:n.93+1022G=
ENST00000415684.5:c.1280G= (TSEN2)	ENSP00000416510.1:p.Trp427=
ENST00000454502.6:c.1181G= (TSEN2)	ENSP00000392029.2:p.Trp394=
ENST00000455118.5:c.205G= (TSEN2)
ENST00000473755.5:n.3363G= (TSEN2)
ENST00000475595.1:n.204G= (TSEN2)
ENST00000567514.1:n.715+6826C= (MKRN2OS)
NM_001145392.1:c.1358G= (TSEN2)	NP_001138864.1:p.Trp453=
NM_001145393.1:c.1280G= (TSEN2)	NP_001138865.1:p.Trp427=
NM_001145394.1:c.1181G= (TSEN2)	NP_001138866.1:p.Trp394=
NM_025265.3:c.1358G= (TSEN2)	NP_079541.1:p.Trp453=
XM_005265495.1:c.1358G= (TSEN2)	XP_005265552.1:p.Trp453=
XM_005265497.1:c.1280G= (TSEN2)	XP_005265554.1:p.Trp427=
XM_005265498.1:c.1229G= (TSEN2)	XP_005265555.1:p.Trp410=
XM_011534138.1:c.1091G= (TSEN2)	XP_011532440.1:p.Trp364=
XM_011534139.1:c.1085G= (TSEN2)	XP_011532441.1:p.Trp362=
XR_245158.1:n.1461G= (TSEN2)
XR_245159.3:n.1461G= (TSEN2)
XR_427295.2:n.3363G= (TSEN2)
XR_427296.1:n.1271G= (TSEN2)
NM_001145393.2:c.1280G= (TSEN2)	NP_001138865.1:p.Trp427=
NM_001321277.1:c.1358G= (TSEN2)	NP_001308206.1:p.Trp453=
NM_001321278.1:c.1338+1022G= (TSEN2)	NP_001308207.1:n.1338+1022G=
NM_001321279.1:c.1280G= (TSEN2)	NP_001308208.1:p.Trp427=
NR_135607.1:n.1461G= (TSEN2)
XM_011534139.3:c.1085G= (TSEN2)	XP_011532441.1:p.Trp362=
XM_017007292.1:c.1415G= (TSEN2)	XP_016862781.1:p.Trp472=
XM_017007293.1:c.1415G= (TSEN2)	XP_016862782.1:p.Trp472=
XM_017007294.1:c.1415G= (TSEN2)	XP_016862783.1:p.Trp472=
XM_017007295.2:c.1415G= (TSEN2)	XP_016862784.1:p.Trp472=
XM_017007296.2:c.1358G= (TSEN2)	XP_016862785.1:p.Trp453=
XM_017007297.1:c.1337G= (TSEN2)	XP_016862786.1:p.Trp446=
XM_024453785.1:c.1280G= (TSEN2)	XP_024309553.1:p.Trp427=
XR_001740287.1:n.1802G= (TSEN2)
XR_001740288.2:n.1802G= (TSEN2)
XR_001740289.2:n.1745G= (TSEN2)
XR_001740290.2:n.1359G= (TSEN2)
XR_001740291.1:n.1667G= (TSEN2)
XR_001740292.1:n.1765G= (TSEN2)
XR_001740293.1:n.1765G= (TSEN2)
XR_001740294.2:n.1400G= (TSEN2)
XR_001740295.2:n.1322G= (TSEN2)
XR_001740296.1:n.1612G= (TSEN2)
XR_001740297.1:n.1930G= (TSEN2)
XR_001740298.2:n.1247G= (TSEN2)
XR_001740300.2:n.1565G= (TSEN2)
XR_001740301.2:n.1565G= (TSEN2)
XR_001740302.2:n.1528G= (TSEN2)
XR_001740303.2:n.1375G= (TSEN2)
XR_001740304.1:n.1683G= (TSEN2)
XR_002959592.1:n.1536G= (TSEN2)
XR_002959593.1:n.1493G= (TSEN2)
XR_002959594.1:n.1533G= (TSEN2)
XR_002959595.1:n.1873G= (TSEN2)
XR_427296.2:n.1247G= (TSEN2)
NM_001321278.2:c.1338+1022G= (TSEN2)	NP_001308207.1:n.1338+1022G=
NM_025265.4:c.1358G= (TSEN2) MANE Select	NP_079541.1:p.Trp453=
NR_135607.2:n.1413G= (TSEN2)
NM_001145392.2:c.1358G= (TSEN2)	NP_001138864.1:p.Trp453=
NM_001145393.3:c.1280G= (TSEN2)	NP_001138865.1:p.Trp427=
NM_001145394.2:c.1181G= (TSEN2)	NP_001138866.1:p.Trp394=
NM_001321277.2:c.1358G= (TSEN2)	NP_001308206.1:p.Trp453=
NM_001321279.2:c.1280G= (TSEN2)	NP_001308208.1:p.Trp427=