Canonical Allele Identifier: CA2574628493

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95684526dup , CM000672.2:g.95684526dup	GRCh38
NC_000010.10:g.97444283dup , CM000672.1:g.97444283dup	GRCh37
NC_000010.9:g.97434273dup	NCBI36
NG_032953.1:g.14618dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1068dup MANE Select	ENSP00000360261.5:p.Gln357ThrfsTer23
ENST00000614499.5:c.1122dup	ENSP00000483364.2:p.Gln375ThrfsTer23
ENST00000679485.1:n.1092dup
ENST00000679984.1:c.*323dup	ENSP00000504998.1:n.*323dup
ENST00000680144.1:c.987dup	ENSP00000506398.1:p.Gln330ThrfsTer23
ENST00000680353.1:c.1068dup	ENSP00000505367.1:p.Gln357ThrfsTer23
ENST00000680697.1:n.641dup
ENST00000680709.1:c.831dup	ENSP00000505830.1:p.Gln278ThrfsTer23
ENST00000681127.1:n.2910dup
ENST00000681739.1:n.1123dup
ENST00000681928.1:c.*130+2518dup	ENSP00000505552.1:n.*130+2518dup
ENST00000265993.13:c.1122dup	ENSP00000265993.9:p.Gln375ThrfsTer23
ENST00000371209.5:c.1068dup	ENSP00000360253.5:p.Gln357ThrfsTer23
ENST00000371217.9:c.1068dup	ENSP00000360261.5:p.Gln357ThrfsTer23
ENST00000430368.6:c.652-897dup	ENSP00000387567.1:n.652-897dup
ENST00000614499.4:c.1068dup	ENSP00000483364.1:p.Gln357ThrfsTer23
NM_001143973.1:c.652-897dup	NP_001137445.1:n.652-897dup
NM_015631.5:c.1068dup	NP_056446.4:p.Gln357ThrfsTer23
XM_005269690.1:c.1041dup	XP_005269747.1:p.Gln348ThrfsTer23
XM_011539627.1:c.1122dup	XP_011537929.1:p.Gln375ThrfsTer23
XM_011539628.1:c.1122dup	XP_011537930.1:p.Gln375ThrfsTer23
XM_005269690.2:c.1041dup	XP_005269747.1:p.Gln348ThrfsTer23
XM_011539627.2:c.1122dup	XP_011537929.1:p.Gln375ThrfsTer23
XM_011539628.2:c.1122dup	XP_011537930.1:p.Gln375ThrfsTer23
XM_024447935.1:c.1041dup	XP_024303703.1:p.Gln348ThrfsTer23
NM_015631.6:c.1068dup MANE Select	NP_056446.4:p.Gln357ThrfsTer23
NM_001143973.2:c.652-897dup	NP_001137445.1:n.652-897dup