Canonical Allele Identifier: CA2740093491

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95682733_95682736dup , CM000672.2:g.95682733_95682736dup	GRCh38
NC_000010.10:g.97442490_97442493dup , CM000672.1:g.97442490_97442493dup	GRCh37
NC_000010.9:g.97432480_97432483dup	NCBI36
NG_032953.1:g.16408_16411dup

Transcript Alleles

HGVS	Amino-acid Change
NM_015631.6:c.1367_1370dup MANE Select	NP_056446.4:p.Glu457AspfsTer9
ENST00000371217.10:c.1367_1370dup MANE Select	ENSP00000360261.5:p.Glu457AspfsTer9
NM_001143973.1:c.923_926dup	NP_001137445.1:p.Glu309AspfsTer9
NM_001143973.2:c.923_926dup	NP_001137445.1:p.Glu309AspfsTer9
NM_015631.5:c.1367_1370dup	NP_056446.4:p.Glu457AspfsTer9
ENST00000265993.13:c.1421_1424dup	ENSP00000265993.9:p.Glu475AspfsTer9
ENST00000371217.9:c.1367_1370dup	ENSP00000360261.5:p.Glu457AspfsTer9
ENST00000430368.6:c.923_926dup	ENSP00000387567.1:p.Glu309AspfsTer9
ENST00000614499.4:c.1367_1370dup	ENSP00000483364.1:p.Glu457AspfsTer9
ENST00000614499.5:c.1406_1409dup	ENSP00000483364.2:p.Glu470AspfsTer9
ENST00000679485.1:n.1391_1394dup
ENST00000679984.1:c.*607_*610dup	ENSP00000504998.1:n.*607_*610dup
ENST00000680144.1:c.1271_1274dup	ENSP00000506398.1:p.Glu425AspfsTer9
ENST00000680353.1:c.1203+786_1203+789dup	ENSP00000505367.1:n.1203+786_1203+789dup
ENST00000680697.1:n.1562_1565dup
ENST00000680709.1:c.1115_1118dup	ENSP00000505830.1:p.Glu373AspfsTer9
ENST00000681739.1:n.1748_1751dup
ENST00000681928.1:c.*130+4308_*130+4311dup	ENSP00000505552.1:n.*130+4308_*130+4311dup
XM_005269690.1:c.1340_1343dup	XP_005269747.1:p.Glu448AspfsTer9
XM_005269690.2:c.1340_1343dup	XP_005269747.1:p.Glu448AspfsTer9
XM_011539627.1:c.1406_1409dup	XP_011537929.1:p.Glu470AspfsTer9
XM_011539627.2:c.1406_1409dup	XP_011537929.1:p.Glu470AspfsTer9
XM_011539628.1:c.1421_1424dup	XP_011537930.1:p.Glu475AspfsTer9
XM_011539628.2:c.1421_1424dup	XP_011537930.1:p.Glu475AspfsTer9
XM_024447935.1:c.1325_1328dup	XP_024303703.1:p.Glu443AspfsTer9