Canonical Allele Identifier: CA351478513

Gene: TSEN2 MKRN2OS

Linked Data

• MyVariant Identifiers: chr3:g.12574201G>C (hg19) ; chr3:g.12532702G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12532702G>C , CM000665.2:g.12532702G>C	GRCh38
NC_000003.11:g.12574201G>C , CM000665.1:g.12574201G>C	GRCh37
NC_000003.10:g.12549201G>C	NCBI36
NG_011521.1:g.53271G>C
NG_011521.2:g.53271G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284995.11:c.1379G>C (TSEN2) MANE Select	ENSP00000284995.6:p.Ser460Thr
ENST00000412698.3:c.1260+1043G>C (TSEN2)	ENSP00000408528.3:n.1260+1043G>C
ENST00000415684.6:c.1301G>C (TSEN2)	ENSP00000416510.1:p.Ser434Thr
ENST00000444864.6:c.1260+1043G>C (TSEN2)	ENSP00000407974.2:n.1260+1043G>C
ENST00000446004.6:c.1338+1043G>C (TSEN2)	ENSP00000406238.2:n.1338+1043G>C
ENST00000455118.6:c.*220G>C (TSEN2)	ENSP00000408744.2:n.*220G>C
ENST00000475595.2:n.4062G>C (TSEN2)
ENST00000679367.1:c.*998G>C (TSEN2)	ENSP00000506510.1:n.*998G>C
ENST00000679420.1:n.1552G>C (TSEN2)
ENST00000679424.1:c.*1222G>C (TSEN2)	ENSP00000505917.1:n.*1222G>C
ENST00000679425.1:c.1379G>C (TSEN2)	ENSP00000505890.1:p.Ser460Thr
ENST00000679492.1:c.1338+1043G>C (TSEN2)	ENSP00000505331.1:n.1338+1043G>C
ENST00000679555.1:c.*1102G>C (TSEN2)	ENSP00000505538.1:n.*1102G>C
ENST00000679670.1:c.1301G>C (TSEN2)	ENSP00000506080.1:p.Ser434Thr
ENST00000679690.1:c.*378G>C (TSEN2)	ENSP00000506383.1:n.*378G>C
ENST00000679693.1:c.*175+1043G>C (TSEN2)	ENSP00000505108.1:n.*175+1043G>C
ENST00000679699.1:c.1379G>C (TSEN2)	ENSP00000505274.1:p.Ser460Thr
ENST00000679756.1:c.1328G>C (TSEN2)	ENSP00000506391.1:p.Ser443Thr
ENST00000679785.1:c.*220G>C (TSEN2)	ENSP00000506473.1:n.*220G>C
ENST00000679835.1:c.*568G>C (TSEN2)	ENSP00000505616.1:n.*568G>C
ENST00000679876.1:c.1209+1043G>C (TSEN2)	ENSP00000504930.1:n.1209+1043G>C
ENST00000679995.1:c.*220G>C (TSEN2)	ENSP00000505221.1:n.*220G>C
ENST00000680126.1:c.*1218G>C (TSEN2)	ENSP00000505345.1:n.*1218G>C
ENST00000680264.1:c.*527+1043G>C (TSEN2)	ENSP00000505273.1:n.*527+1043G>C
ENST00000680275.1:c.1436G>C (TSEN2)	ENSP00000505417.1:p.Ser479Thr
ENST00000680354.1:c.1358G>C (TSEN2)	ENSP00000505106.1:p.Ser453Thr
ENST00000680376.1:c.*568G>C (TSEN2)	ENSP00000506369.1:n.*568G>C
ENST00000680421.1:c.1250G>C (TSEN2)	ENSP00000505530.1:p.Ser417Thr
ENST00000680449.1:c.*521G>C (TSEN2)	ENSP00000505709.1:n.*521G>C
ENST00000680458.1:c.*194G>C (TSEN2)	ENSP00000505979.1:n.*194G>C
ENST00000680555.1:c.*220G>C (TSEN2)	ENSP00000505160.1:n.*220G>C
ENST00000680598.1:c.1328G>C (TSEN2)	ENSP00000506297.1:p.Ser443Thr
ENST00000680765.1:c.*220G>C (TSEN2)	ENSP00000505351.1:n.*220G>C
ENST00000680817.1:c.1250G>C (TSEN2)	ENSP00000506221.1:p.Ser417Thr
ENST00000680857.1:c.1338+1043G>C (TSEN2)	ENSP00000506578.1:n.1338+1043G>C
ENST00000680873.1:c.*531G>C (TSEN2)	ENSP00000505233.1:n.*531G>C
ENST00000680923.1:c.*568G>C (TSEN2)	ENSP00000505344.1:n.*568G>C
ENST00000680943.1:c.1328G>C (TSEN2)	ENSP00000505442.1:p.Ser443Thr
ENST00000680986.1:c.1379G>C (TSEN2)	ENSP00000505799.1:p.Ser460Thr
ENST00000681042.1:c.1100-6459G>C (TSEN2)	ENSP00000505622.1:n.1100-6459G>C
ENST00000681073.1:c.*220G>C (TSEN2)	ENSP00000506576.1:n.*220G>C
ENST00000681140.1:c.1379G>C (TSEN2)	ENSP00000505099.1:p.Ser460Thr
ENST00000681227.1:c.*251G>C (TSEN2)	ENSP00000505240.1:n.*251G>C
ENST00000681268.1:c.*1523G>C (TSEN2)	ENSP00000505385.1:n.*1523G>C
ENST00000681343.1:c.*998G>C (TSEN2)	ENSP00000506265.1:n.*998G>C
ENST00000681433.1:c.*220G>C (TSEN2)	ENSP00000505729.1:n.*220G>C
ENST00000681471.1:c.1301G>C (TSEN2)	ENSP00000505105.1:p.Ser434Thr
ENST00000681482.1:c.1379G>C (TSEN2)	ENSP00000505436.1:p.Ser460Thr
ENST00000681676.1:c.1301G>C (TSEN2)	ENSP00000506163.1:p.Ser434Thr
ENST00000681713.1:c.*998G>C (TSEN2)	ENSP00000506046.1:n.*998G>C
ENST00000284995.10:c.1379G>C (TSEN2)	ENSP00000284995.6:p.Ser460Thr
ENST00000402228.7:c.1379G>C (TSEN2)	ENSP00000385976.3:p.Ser460Thr
ENST00000412698.2:c.93+1043G>C (TSEN2)	ENSP00000408528.2:n.93+1043G>C
ENST00000415684.5:c.1301G>C (TSEN2)	ENSP00000416510.1:p.Ser434Thr
ENST00000454502.6:c.1202G>C (TSEN2)	ENSP00000392029.2:p.Ser401Thr
ENST00000455118.5:c.226G>C (TSEN2)
ENST00000473755.5:n.3384G>C (TSEN2)
ENST00000475595.1:n.225G>C (TSEN2)
ENST00000567514.1:n.715+6805C>G (MKRN2OS)
NM_001145392.1:c.1379G>C (TSEN2)	NP_001138864.1:p.Ser460Thr
NM_001145393.1:c.1301G>C (TSEN2)	NP_001138865.1:p.Ser434Thr
NM_001145394.1:c.1202G>C (TSEN2)	NP_001138866.1:p.Ser401Thr
NM_025265.3:c.1379G>C (TSEN2)	NP_079541.1:p.Ser460Thr
XM_005265495.1:c.1379G>C (TSEN2)	XP_005265552.1:p.Ser460Thr
XM_005265497.1:c.1301G>C (TSEN2)	XP_005265554.1:p.Ser434Thr
XM_005265498.1:c.1250G>C (TSEN2)	XP_005265555.1:p.Ser417Thr
XM_011534138.1:c.1112G>C (TSEN2)	XP_011532440.1:p.Ser371Thr
XM_011534139.1:c.1106G>C (TSEN2)	XP_011532441.1:p.Ser369Thr
XR_245158.1:n.1482G>C (TSEN2)
XR_245159.3:n.1482G>C (TSEN2)
XR_427295.2:n.3384G>C (TSEN2)
XR_427296.1:n.1292G>C (TSEN2)
NM_001145393.2:c.1301G>C (TSEN2)	NP_001138865.1:p.Ser434Thr
NM_001321277.1:c.1379G>C (TSEN2)	NP_001308206.1:p.Ser460Thr
NM_001321278.1:c.1338+1043G>C (TSEN2)	NP_001308207.1:n.1338+1043G>C
NM_001321279.1:c.1301G>C (TSEN2)	NP_001308208.1:p.Ser434Thr
NR_135607.1:n.1482G>C (TSEN2)
XM_011534139.3:c.1106G>C (TSEN2)	XP_011532441.1:p.Ser369Thr
XM_017007292.1:c.1436G>C (TSEN2)	XP_016862781.1:p.Ser479Thr
XM_017007293.1:c.1436G>C (TSEN2)	XP_016862782.1:p.Ser479Thr
XM_017007294.1:c.1436G>C (TSEN2)	XP_016862783.1:p.Ser479Thr
XM_017007295.2:c.1436G>C (TSEN2)	XP_016862784.1:p.Ser479Thr
XM_017007296.2:c.1379G>C (TSEN2)	XP_016862785.1:p.Ser460Thr
XM_017007297.1:c.1358G>C (TSEN2)	XP_016862786.1:p.Ser453Thr
XM_024453785.1:c.1301G>C (TSEN2)	XP_024309553.1:p.Ser434Thr
XR_001740287.1:n.1823G>C (TSEN2)
XR_001740288.2:n.1823G>C (TSEN2)
XR_001740289.2:n.1766G>C (TSEN2)
XR_001740290.2:n.1380G>C (TSEN2)
XR_001740291.1:n.1688G>C (TSEN2)
XR_001740292.1:n.1786G>C (TSEN2)
XR_001740293.1:n.1786G>C (TSEN2)
XR_001740294.2:n.1421G>C (TSEN2)
XR_001740295.2:n.1343G>C (TSEN2)
XR_001740296.1:n.1633G>C (TSEN2)
XR_001740297.1:n.1951G>C (TSEN2)
XR_001740298.2:n.1268G>C (TSEN2)
XR_001740300.2:n.1586G>C (TSEN2)
XR_001740301.2:n.1586G>C (TSEN2)
XR_001740302.2:n.1549G>C (TSEN2)
XR_001740303.2:n.1396G>C (TSEN2)
XR_001740304.1:n.1704G>C (TSEN2)
XR_002959592.1:n.1557G>C (TSEN2)
XR_002959593.1:n.1514G>C (TSEN2)
XR_002959594.1:n.1554G>C (TSEN2)
XR_002959595.1:n.1894G>C (TSEN2)
XR_427296.2:n.1268G>C (TSEN2)
NM_001321278.2:c.1338+1043G>C (TSEN2)	NP_001308207.1:n.1338+1043G>C
NM_025265.4:c.1379G>C (TSEN2) MANE Select	NP_079541.1:p.Ser460Thr
NR_135607.2:n.1434G>C (TSEN2)
NM_001145392.2:c.1379G>C (TSEN2)	NP_001138864.1:p.Ser460Thr
NM_001145393.3:c.1301G>C (TSEN2)	NP_001138865.1:p.Ser434Thr
NM_001145394.2:c.1202G>C (TSEN2)	NP_001138866.1:p.Ser401Thr
NM_001321277.2:c.1379G>C (TSEN2)	NP_001308206.1:p.Ser460Thr
NM_001321279.2:c.1301G>C (TSEN2)	NP_001308208.1:p.Ser434Thr