Canonical Allele Identifier: CA2574628579

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95687103dup , CM000672.2:g.95687103dup	GRCh38
NC_000010.10:g.97446860dup , CM000672.1:g.97446860dup	GRCh37
NC_000010.9:g.97436850dup	NCBI36
NG_032953.1:g.12041dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.793dup MANE Select	ENSP00000360261.5:p.Ser265LysfsTer15
ENST00000614499.5:c.847dup	ENSP00000483364.2:p.Ser283LysfsTer15
ENST00000679485.1:n.817dup
ENST00000679566.1:c.793dup	ENSP00000505964.1:p.Ser265LysfsTer15
ENST00000679984.1:c.*48dup	ENSP00000504998.1:n.*48dup
ENST00000680144.1:c.793dup	ENSP00000506398.1:p.Ser265LysfsTer15
ENST00000680353.1:c.793dup	ENSP00000505367.1:p.Ser265LysfsTer15
ENST00000680697.1:n.543-2479dup
ENST00000680709.1:c.556dup	ENSP00000505830.1:p.Ser186LysfsTer15
ENST00000681127.1:n.846dup
ENST00000681739.1:n.848dup
ENST00000681928.1:c.*71dup	ENSP00000505552.1:n.*71dup
ENST00000265993.13:c.847dup	ENSP00000265993.9:p.Ser283LysfsTer15
ENST00000371209.5:c.793dup	ENSP00000360253.5:p.Ser265LysfsTer15
ENST00000371217.9:c.793dup	ENSP00000360261.5:p.Ser265LysfsTer15
ENST00000430368.6:c.556dup	ENSP00000387567.1:p.Ser186LysfsTer15
ENST00000497399.1:n.779dup
ENST00000614499.4:c.793dup	ENSP00000483364.1:p.Ser265LysfsTer15
NM_001143973.1:c.556dup	NP_001137445.1:p.Ser186LysfsTer15
NM_015631.5:c.793dup	NP_056446.4:p.Ser265LysfsTer15
XM_005269690.1:c.847dup	XP_005269747.1:p.Ser283LysfsTer15
XM_011539627.1:c.847dup	XP_011537929.1:p.Ser283LysfsTer15
XM_011539628.1:c.847dup	XP_011537930.1:p.Ser283LysfsTer15
XM_005269690.2:c.847dup	XP_005269747.1:p.Ser283LysfsTer15
XM_011539627.2:c.847dup	XP_011537929.1:p.Ser283LysfsTer15
XM_011539628.2:c.847dup	XP_011537930.1:p.Ser283LysfsTer15
XM_024447935.1:c.847dup	XP_024303703.1:p.Ser283LysfsTer15
NM_015631.6:c.793dup MANE Select	NP_056446.4:p.Ser265LysfsTer15
NM_001143973.2:c.556dup	NP_001137445.1:p.Ser186LysfsTer15