Canonical Allele Identifier: CA1346196810

Gene: TSEN2 MKRN2OS

Linked Data

• dbSNP Id: rs2057545441

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12532753C>G , CM000665.2:g.12532753C>G	GRCh38
NC_000003.11:g.12574252C>G , CM000665.1:g.12574252C>G	GRCh37
NC_000003.10:g.12549252C>G	NCBI36
NG_011521.1:g.53322C>G
NG_011521.2:g.53322C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284995.11:c.*32C>G (TSEN2) MANE Select	ENSP00000284995.6:n.*32C>G
ENST00000412698.3:c.1260+1094C>G (TSEN2)	ENSP00000408528.3:n.1260+1094C>G
ENST00000415684.6:c.*32C>G (TSEN2)	ENSP00000416510.1:n.*32C>G
ENST00000444864.6:c.1260+1094C>G (TSEN2)	ENSP00000407974.2:n.1260+1094C>G
ENST00000446004.6:c.1338+1094C>G (TSEN2)	ENSP00000406238.2:n.1338+1094C>G
ENST00000455118.6:c.*271C>G (TSEN2)	ENSP00000408744.2:n.*271C>G
ENST00000475595.2:n.4113C>G (TSEN2)
ENST00000679367.1:c.*1049C>G (TSEN2)	ENSP00000506510.1:n.*1049C>G
ENST00000679420.1:n.1603C>G (TSEN2)
ENST00000679424.1:c.*1273C>G (TSEN2)	ENSP00000505917.1:n.*1273C>G
ENST00000679425.1:c.*32C>G (TSEN2)	ENSP00000505890.1:n.*32C>G
ENST00000679492.1:c.1338+1094C>G (TSEN2)	ENSP00000505331.1:n.1338+1094C>G
ENST00000679555.1:c.*1153C>G (TSEN2)	ENSP00000505538.1:n.*1153C>G
ENST00000679670.1:c.*32C>G (TSEN2)	ENSP00000506080.1:n.*32C>G
ENST00000679690.1:c.*429C>G (TSEN2)	ENSP00000506383.1:n.*429C>G
ENST00000679693.1:c.*175+1094C>G (TSEN2)	ENSP00000505108.1:n.*175+1094C>G
ENST00000679699.1:c.*32C>G (TSEN2)	ENSP00000505274.1:n.*32C>G
ENST00000679756.1:c.*32C>G (TSEN2)	ENSP00000506391.1:n.*32C>G
ENST00000679785.1:c.*271C>G (TSEN2)	ENSP00000506473.1:n.*271C>G
ENST00000679835.1:c.*619C>G (TSEN2)	ENSP00000505616.1:n.*619C>G
ENST00000679876.1:c.1209+1094C>G (TSEN2)	ENSP00000504930.1:n.1209+1094C>G
ENST00000679995.1:c.*271C>G (TSEN2)	ENSP00000505221.1:n.*271C>G
ENST00000680126.1:c.*1269C>G (TSEN2)	ENSP00000505345.1:n.*1269C>G
ENST00000680264.1:c.*527+1094C>G (TSEN2)	ENSP00000505273.1:n.*527+1094C>G
ENST00000680275.1:c.*32C>G (TSEN2)	ENSP00000505417.1:n.*32C>G
ENST00000680354.1:c.1409C>G (TSEN2)	ENSP00000505106.1:n.1409C>G
ENST00000680376.1:c.*619C>G (TSEN2)	ENSP00000506369.1:n.*619C>G
ENST00000680421.1:c.*32C>G (TSEN2)	ENSP00000505530.1:n.*32C>G
ENST00000680449.1:c.*572C>G (TSEN2)	ENSP00000505709.1:n.*572C>G
ENST00000680458.1:c.*245C>G (TSEN2)	ENSP00000505979.1:n.*245C>G
ENST00000680555.1:c.*271C>G (TSEN2)	ENSP00000505160.1:n.*271C>G
ENST00000680598.1:c.*32C>G (TSEN2)	ENSP00000506297.1:n.*32C>G
ENST00000680765.1:c.*271C>G (TSEN2)	ENSP00000505351.1:n.*271C>G
ENST00000680817.1:c.*32C>G (TSEN2)	ENSP00000506221.1:n.*32C>G
ENST00000680857.1:c.1338+1094C>G (TSEN2)	ENSP00000506578.1:n.1338+1094C>G
ENST00000680873.1:c.*582C>G (TSEN2)	ENSP00000505233.1:n.*582C>G
ENST00000680923.1:c.*619C>G (TSEN2)	ENSP00000505344.1:n.*619C>G
ENST00000680943.1:c.*32C>G (TSEN2)	ENSP00000505442.1:n.*32C>G
ENST00000680986.1:c.*32C>G (TSEN2)	ENSP00000505799.1:n.*32C>G
ENST00000681042.1:c.1100-6408C>G (TSEN2)	ENSP00000505622.1:n.1100-6408C>G
ENST00000681073.1:c.*271C>G (TSEN2)	ENSP00000506576.1:n.*271C>G
ENST00000681140.1:c.*32C>G (TSEN2)	ENSP00000505099.1:n.*32C>G
ENST00000681227.1:c.*302C>G (TSEN2)	ENSP00000505240.1:n.*302C>G
ENST00000681268.1:c.*1574C>G (TSEN2)	ENSP00000505385.1:n.*1574C>G
ENST00000681343.1:c.*1049C>G (TSEN2)	ENSP00000506265.1:n.*1049C>G
ENST00000681433.1:c.*271C>G (TSEN2)	ENSP00000505729.1:n.*271C>G
ENST00000681471.1:c.*32C>G (TSEN2)	ENSP00000505105.1:n.*32C>G
ENST00000681482.1:c.*32C>G (TSEN2)	ENSP00000505436.1:n.*32C>G
ENST00000681676.1:c.*32C>G (TSEN2)	ENSP00000506163.1:n.*32C>G
ENST00000681713.1:c.*1049C>G (TSEN2)	ENSP00000506046.1:n.*1049C>G
ENST00000284995.10:c.*32C>G (TSEN2)	ENSP00000284995.6:n.*32C>G
ENST00000402228.7:c.*32C>G (TSEN2)	ENSP00000385976.3:n.*32C>G
ENST00000412698.2:c.93+1094C>G (TSEN2)	ENSP00000408528.2:n.93+1094C>G
ENST00000415684.5:c.*32C>G (TSEN2)	ENSP00000416510.1:n.*32C>G
ENST00000454502.6:c.*32C>G (TSEN2)	ENSP00000392029.2:n.*32C>G
ENST00000455118.5:c.277C>G (TSEN2)
ENST00000473755.5:n.3435C>G (TSEN2)
ENST00000475595.1:n.276C>G (TSEN2)
ENST00000567514.1:n.715+6754G>C (MKRN2OS)
NM_001145392.1:c.*32C>G (TSEN2)	NP_001138864.1:n.*32C>G
NM_001145393.1:c.*32C>G (TSEN2)	NP_001138865.1:n.*32C>G
NM_001145394.1:c.*32C>G (TSEN2)	NP_001138866.1:n.*32C>G
NM_025265.3:c.*32C>G (TSEN2)	NP_079541.1:n.*32C>G
XM_005265495.1:c.*32C>G (TSEN2)	XP_005265552.1:n.*32C>G
XM_005265497.1:c.*32C>G (TSEN2)	XP_005265554.1:n.*32C>G
XM_005265498.1:c.*32C>G (TSEN2)	XP_005265555.1:n.*32C>G
XM_011534138.1:c.*32C>G (TSEN2)	XP_011532440.1:n.*32C>G
XM_011534139.1:c.*32C>G (TSEN2)	XP_011532441.1:n.*32C>G
XR_245158.1:n.1533C>G (TSEN2)
XR_245159.3:n.1533C>G (TSEN2)
XR_427295.2:n.3435C>G (TSEN2)
XR_427296.1:n.1343C>G (TSEN2)
NM_001145393.2:c.*32C>G (TSEN2)	NP_001138865.1:n.*32C>G
NM_001321277.1:c.*32C>G (TSEN2)	NP_001308206.1:n.*32C>G
NM_001321278.1:c.1338+1094C>G (TSEN2)	NP_001308207.1:n.1338+1094C>G
NM_001321279.1:c.*32C>G (TSEN2)	NP_001308208.1:n.*32C>G
NR_135607.1:n.1533C>G (TSEN2)
XM_011534139.3:c.*32C>G (TSEN2)	XP_011532441.1:n.*32C>G
XM_017007292.1:c.*32C>G (TSEN2)	XP_016862781.1:n.*32C>G
XM_017007293.1:c.*32C>G (TSEN2)	XP_016862782.1:n.*32C>G
XM_017007294.1:c.*32C>G (TSEN2)	XP_016862783.1:n.*32C>G
XM_017007295.2:c.*32C>G (TSEN2)	XP_016862784.1:n.*32C>G
XM_017007296.2:c.*32C>G (TSEN2)	XP_016862785.1:n.*32C>G
XM_017007297.1:c.*32C>G (TSEN2)	XP_016862786.1:n.*32C>G
XM_024453785.1:c.*32C>G (TSEN2)	XP_024309553.1:n.*32C>G
XR_001740287.1:n.1874C>G (TSEN2)
XR_001740288.2:n.1874C>G (TSEN2)
XR_001740289.2:n.1817C>G (TSEN2)
XR_001740290.2:n.1431C>G (TSEN2)
XR_001740291.1:n.1739C>G (TSEN2)
XR_001740292.1:n.1837C>G (TSEN2)
XR_001740293.1:n.1837C>G (TSEN2)
XR_001740294.2:n.1472C>G (TSEN2)
XR_001740295.2:n.1394C>G (TSEN2)
XR_001740296.1:n.1684C>G (TSEN2)
XR_001740297.1:n.2002C>G (TSEN2)
XR_001740298.2:n.1319C>G (TSEN2)
XR_001740300.2:n.1637C>G (TSEN2)
XR_001740301.2:n.1637C>G (TSEN2)
XR_001740302.2:n.1600C>G (TSEN2)
XR_001740303.2:n.1447C>G (TSEN2)
XR_001740304.1:n.1755C>G (TSEN2)
XR_002959592.1:n.1608C>G (TSEN2)
XR_002959593.1:n.1565C>G (TSEN2)
XR_002959594.1:n.1605C>G (TSEN2)
XR_002959595.1:n.1945C>G (TSEN2)
XR_427296.2:n.1319C>G (TSEN2)
NM_001321278.2:c.1338+1094C>G (TSEN2)	NP_001308207.1:n.1338+1094C>G
NM_025265.4:c.*32C>G (TSEN2) MANE Select	NP_079541.1:n.*32C>G
NR_135607.2:n.1485C>G (TSEN2)
NM_001145392.2:c.*32C>G (TSEN2)	NP_001138864.1:n.*32C>G
NM_001145393.3:c.*32C>G (TSEN2)	NP_001138865.1:n.*32C>G
NM_001145394.2:c.*32C>G (TSEN2)	NP_001138866.1:n.*32C>G
NM_001321277.2:c.*32C>G (TSEN2)	NP_001308206.1:n.*32C>G
NM_001321279.2:c.*32C>G (TSEN2)	NP_001308208.1:n.*32C>G