Canonical Allele Identifier: CA351478469

Gene: TSEN2 MKRN2OS

Linked Data

• MyVariant Identifiers: chr3:g.12574192G>C (hg19) ; chr3:g.12532693G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12532693G>C , CM000665.2:g.12532693G>C	GRCh38
NC_000003.11:g.12574192G>C , CM000665.1:g.12574192G>C	GRCh37
NC_000003.10:g.12549192G>C	NCBI36
NG_011521.1:g.53262G>C
NG_011521.2:g.53262G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284995.11:c.1370G>C (TSEN2) MANE Select	ENSP00000284995.6:p.Arg457Pro
ENST00000412698.3:c.1260+1034G>C (TSEN2)	ENSP00000408528.3:n.1260+1034G>C
ENST00000415684.6:c.1292G>C (TSEN2)	ENSP00000416510.1:p.Arg431Pro
ENST00000444864.6:c.1260+1034G>C (TSEN2)	ENSP00000407974.2:n.1260+1034G>C
ENST00000446004.6:c.1338+1034G>C (TSEN2)	ENSP00000406238.2:n.1338+1034G>C
ENST00000455118.6:c.*211G>C (TSEN2)	ENSP00000408744.2:n.*211G>C
ENST00000475595.2:n.4053G>C (TSEN2)
ENST00000679367.1:c.*989G>C (TSEN2)	ENSP00000506510.1:n.*989G>C
ENST00000679420.1:n.1543G>C (TSEN2)
ENST00000679424.1:c.*1213G>C (TSEN2)	ENSP00000505917.1:n.*1213G>C
ENST00000679425.1:c.1370G>C (TSEN2)	ENSP00000505890.1:p.Arg457Pro
ENST00000679492.1:c.1338+1034G>C (TSEN2)	ENSP00000505331.1:n.1338+1034G>C
ENST00000679555.1:c.*1093G>C (TSEN2)	ENSP00000505538.1:n.*1093G>C
ENST00000679670.1:c.1292G>C (TSEN2)	ENSP00000506080.1:p.Arg431Pro
ENST00000679690.1:c.*369G>C (TSEN2)	ENSP00000506383.1:n.*369G>C
ENST00000679693.1:c.*175+1034G>C (TSEN2)	ENSP00000505108.1:n.*175+1034G>C
ENST00000679699.1:c.1370G>C (TSEN2)	ENSP00000505274.1:p.Arg457Pro
ENST00000679756.1:c.1319G>C (TSEN2)	ENSP00000506391.1:p.Arg440Pro
ENST00000679785.1:c.*211G>C (TSEN2)	ENSP00000506473.1:n.*211G>C
ENST00000679835.1:c.*559G>C (TSEN2)	ENSP00000505616.1:n.*559G>C
ENST00000679876.1:c.1209+1034G>C (TSEN2)	ENSP00000504930.1:n.1209+1034G>C
ENST00000679995.1:c.*211G>C (TSEN2)	ENSP00000505221.1:n.*211G>C
ENST00000680126.1:c.*1209G>C (TSEN2)	ENSP00000505345.1:n.*1209G>C
ENST00000680264.1:c.*527+1034G>C (TSEN2)	ENSP00000505273.1:n.*527+1034G>C
ENST00000680275.1:c.1427G>C (TSEN2)	ENSP00000505417.1:p.Arg476Pro
ENST00000680354.1:c.1349G>C (TSEN2)	ENSP00000505106.1:p.Arg450Pro
ENST00000680376.1:c.*559G>C (TSEN2)	ENSP00000506369.1:n.*559G>C
ENST00000680421.1:c.1241G>C (TSEN2)	ENSP00000505530.1:p.Arg414Pro
ENST00000680449.1:c.*512G>C (TSEN2)	ENSP00000505709.1:n.*512G>C
ENST00000680458.1:c.*185G>C (TSEN2)	ENSP00000505979.1:n.*185G>C
ENST00000680555.1:c.*211G>C (TSEN2)	ENSP00000505160.1:n.*211G>C
ENST00000680598.1:c.1319G>C (TSEN2)	ENSP00000506297.1:p.Arg440Pro
ENST00000680765.1:c.*211G>C (TSEN2)	ENSP00000505351.1:n.*211G>C
ENST00000680817.1:c.1241G>C (TSEN2)	ENSP00000506221.1:p.Arg414Pro
ENST00000680857.1:c.1338+1034G>C (TSEN2)	ENSP00000506578.1:n.1338+1034G>C
ENST00000680873.1:c.*522G>C (TSEN2)	ENSP00000505233.1:n.*522G>C
ENST00000680923.1:c.*559G>C (TSEN2)	ENSP00000505344.1:n.*559G>C
ENST00000680943.1:c.1319G>C (TSEN2)	ENSP00000505442.1:p.Arg440Pro
ENST00000680986.1:c.1370G>C (TSEN2)	ENSP00000505799.1:p.Arg457Pro
ENST00000681042.1:c.1100-6468G>C (TSEN2)	ENSP00000505622.1:n.1100-6468G>C
ENST00000681073.1:c.*211G>C (TSEN2)	ENSP00000506576.1:n.*211G>C
ENST00000681140.1:c.1370G>C (TSEN2)	ENSP00000505099.1:p.Arg457Pro
ENST00000681227.1:c.*242G>C (TSEN2)	ENSP00000505240.1:n.*242G>C
ENST00000681268.1:c.*1514G>C (TSEN2)	ENSP00000505385.1:n.*1514G>C
ENST00000681343.1:c.*989G>C (TSEN2)	ENSP00000506265.1:n.*989G>C
ENST00000681433.1:c.*211G>C (TSEN2)	ENSP00000505729.1:n.*211G>C
ENST00000681471.1:c.1292G>C (TSEN2)	ENSP00000505105.1:p.Arg431Pro
ENST00000681482.1:c.1370G>C (TSEN2)	ENSP00000505436.1:p.Arg457Pro
ENST00000681676.1:c.1292G>C (TSEN2)	ENSP00000506163.1:p.Arg431Pro
ENST00000681713.1:c.*989G>C (TSEN2)	ENSP00000506046.1:n.*989G>C
ENST00000284995.10:c.1370G>C (TSEN2)	ENSP00000284995.6:p.Arg457Pro
ENST00000402228.7:c.1370G>C (TSEN2)	ENSP00000385976.3:p.Arg457Pro
ENST00000412698.2:c.93+1034G>C (TSEN2)	ENSP00000408528.2:n.93+1034G>C
ENST00000415684.5:c.1292G>C (TSEN2)	ENSP00000416510.1:p.Arg431Pro
ENST00000454502.6:c.1193G>C (TSEN2)	ENSP00000392029.2:p.Arg398Pro
ENST00000455118.5:c.217G>C (TSEN2)
ENST00000473755.5:n.3375G>C (TSEN2)
ENST00000475595.1:n.216G>C (TSEN2)
ENST00000567514.1:n.715+6814C>G (MKRN2OS)
NM_001145392.1:c.1370G>C (TSEN2)	NP_001138864.1:p.Arg457Pro
NM_001145393.1:c.1292G>C (TSEN2)	NP_001138865.1:p.Arg431Pro
NM_001145394.1:c.1193G>C (TSEN2)	NP_001138866.1:p.Arg398Pro
NM_025265.3:c.1370G>C (TSEN2)	NP_079541.1:p.Arg457Pro
XM_005265495.1:c.1370G>C (TSEN2)	XP_005265552.1:p.Arg457Pro
XM_005265497.1:c.1292G>C (TSEN2)	XP_005265554.1:p.Arg431Pro
XM_005265498.1:c.1241G>C (TSEN2)	XP_005265555.1:p.Arg414Pro
XM_011534138.1:c.1103G>C (TSEN2)	XP_011532440.1:p.Arg368Pro
XM_011534139.1:c.1097G>C (TSEN2)	XP_011532441.1:p.Arg366Pro
XR_245158.1:n.1473G>C (TSEN2)
XR_245159.3:n.1473G>C (TSEN2)
XR_427295.2:n.3375G>C (TSEN2)
XR_427296.1:n.1283G>C (TSEN2)
NM_001145393.2:c.1292G>C (TSEN2)	NP_001138865.1:p.Arg431Pro
NM_001321277.1:c.1370G>C (TSEN2)	NP_001308206.1:p.Arg457Pro
NM_001321278.1:c.1338+1034G>C (TSEN2)	NP_001308207.1:n.1338+1034G>C
NM_001321279.1:c.1292G>C (TSEN2)	NP_001308208.1:p.Arg431Pro
NR_135607.1:n.1473G>C (TSEN2)
XM_011534139.3:c.1097G>C (TSEN2)	XP_011532441.1:p.Arg366Pro
XM_017007292.1:c.1427G>C (TSEN2)	XP_016862781.1:p.Arg476Pro
XM_017007293.1:c.1427G>C (TSEN2)	XP_016862782.1:p.Arg476Pro
XM_017007294.1:c.1427G>C (TSEN2)	XP_016862783.1:p.Arg476Pro
XM_017007295.2:c.1427G>C (TSEN2)	XP_016862784.1:p.Arg476Pro
XM_017007296.2:c.1370G>C (TSEN2)	XP_016862785.1:p.Arg457Pro
XM_017007297.1:c.1349G>C (TSEN2)	XP_016862786.1:p.Arg450Pro
XM_024453785.1:c.1292G>C (TSEN2)	XP_024309553.1:p.Arg431Pro
XR_001740287.1:n.1814G>C (TSEN2)
XR_001740288.2:n.1814G>C (TSEN2)
XR_001740289.2:n.1757G>C (TSEN2)
XR_001740290.2:n.1371G>C (TSEN2)
XR_001740291.1:n.1679G>C (TSEN2)
XR_001740292.1:n.1777G>C (TSEN2)
XR_001740293.1:n.1777G>C (TSEN2)
XR_001740294.2:n.1412G>C (TSEN2)
XR_001740295.2:n.1334G>C (TSEN2)
XR_001740296.1:n.1624G>C (TSEN2)
XR_001740297.1:n.1942G>C (TSEN2)
XR_001740298.2:n.1259G>C (TSEN2)
XR_001740300.2:n.1577G>C (TSEN2)
XR_001740301.2:n.1577G>C (TSEN2)
XR_001740302.2:n.1540G>C (TSEN2)
XR_001740303.2:n.1387G>C (TSEN2)
XR_001740304.1:n.1695G>C (TSEN2)
XR_002959592.1:n.1548G>C (TSEN2)
XR_002959593.1:n.1505G>C (TSEN2)
XR_002959594.1:n.1545G>C (TSEN2)
XR_002959595.1:n.1885G>C (TSEN2)
XR_427296.2:n.1259G>C (TSEN2)
NM_001321278.2:c.1338+1034G>C (TSEN2)	NP_001308207.1:n.1338+1034G>C
NM_025265.4:c.1370G>C (TSEN2) MANE Select	NP_079541.1:p.Arg457Pro
NR_135607.2:n.1425G>C (TSEN2)
NM_001145392.2:c.1370G>C (TSEN2)	NP_001138864.1:p.Arg457Pro
NM_001145393.3:c.1292G>C (TSEN2)	NP_001138865.1:p.Arg431Pro
NM_001145394.2:c.1193G>C (TSEN2)	NP_001138866.1:p.Arg398Pro
NM_001321277.2:c.1370G>C (TSEN2)	NP_001308206.1:p.Arg457Pro
NM_001321279.2:c.1292G>C (TSEN2)	NP_001308208.1:p.Arg431Pro