Canonical Allele Identifier: CA5620796

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95680500C>T , CM000672.2:g.95680500C>T	GRCh38
NC_000010.10:g.97440257C>T , CM000672.1:g.97440257C>T	GRCh37
NC_000010.9:g.97430247C>T	NCBI36
NG_032953.1:g.18644G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1562G>A MANE Select	ENSP00000360261.5:p.Arg521Gln
ENST00000614499.5:c.1601G>A	ENSP00000483364.2:p.Arg534Gln
ENST00000679485.1:n.1586G>A
ENST00000679984.1:c.*802G>A	ENSP00000504998.1:n.*802G>A
ENST00000680144.1:c.1466G>A	ENSP00000506398.1:p.Arg489Gln
ENST00000680353.1:c.1313G>A	ENSP00000505367.1:p.Arg438Gln
ENST00000680697.1:n.1757G>A
ENST00000680709.1:c.1310G>A	ENSP00000505830.1:p.Arg437Gln
ENST00000680781.1:c.108G>A
ENST00000681185.1:n.264G>A
ENST00000681739.1:n.1943G>A
ENST00000681928.1:c.*130+6544G>A	ENSP00000505552.1:n.*130+6544G>A
ENST00000265993.13:c.1616G>A	ENSP00000265993.9:p.Arg539Gln
ENST00000371217.9:c.1562G>A	ENSP00000360261.5:p.Arg521Gln
ENST00000430368.6:c.1118G>A	ENSP00000387567.1:p.Arg373Gln
ENST00000614499.4:c.1562G>A	ENSP00000483364.1:p.Arg521Gln
NM_001143973.1:c.1118G>A	NP_001137445.1:p.Arg373Gln
NM_015631.5:c.1562G>A	NP_056446.4:p.Arg521Gln
XM_005269690.1:c.1535G>A	XP_005269747.1:p.Arg512Gln
XM_011539627.1:c.1601G>A	XP_011537929.1:p.Arg534Gln
XM_011539628.1:c.1506+2151G>A	XP_011537930.1:n.1506+2151G>A
XM_005269690.2:c.1535G>A	XP_005269747.1:p.Arg512Gln
XM_011539627.2:c.1601G>A	XP_011537929.1:p.Arg534Gln
XM_011539628.2:c.1506+2151G>A	XP_011537930.1:n.1506+2151G>A
XM_024447935.1:c.1520G>A	XP_024303703.1:p.Arg507Gln
NM_015631.6:c.1562G>A MANE Select	NP_056446.4:p.Arg521Gln
NM_001143973.2:c.1118G>A	NP_001137445.1:p.Arg373Gln