Canonical Allele Identifier: CA1310518146

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532251G= , CM000664.2:g.178532251G=	GRCh38
NC_000002.11:g.179396978G= , CM000664.1:g.179396978G=	GRCh37
NC_000002.10:g.179105224G=	NCBI36
NG_011618.3:g.303552C= , LRG_391:g.303552C=
NG_051363.1:g.14425G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96660C= (TTN)	ENSP00000343764.6:p.Ser32220=
ENST00000342175.11:c.77745C= (TTN)	ENSP00000340554.6:p.Ser25915=
ENST00000359218.10:c.77544C= (TTN)	ENSP00000352154.5:p.Ser25848=
ENST00000342175.10:c.77745C= (TTN)	ENSP00000340554.6:p.Ser25915=
ENST00000342992.10:c.96660C= (TTN)	ENSP00000343764.6:p.Ser32220=
ENST00000359218.9:c.77544C= (TTN)	ENSP00000352154.5:p.Ser25848=
ENST00000460472.6:c.77169C= (TTN)	ENSP00000434586.1:p.Ser25723=
ENST00000589042.5:c.104364C= (TTN) MANE Select	ENSP00000467141.1:p.Ser34788=
ENST00000591111.5:c.99441C= (TTN)	ENSP00000465570.1:p.Ser33147=
ENST00000615779.4:c.99441C= (TTN)	ENSP00000483597.1:p.Ser33147=
NM_001256850.1:c.99441C= (TTN)	NP_001243779.1:p.Ser33147=
NM_001267550.2:c.104364C= (TTN) MANE Select	NP_001254479.2:p.Ser34788=
NM_003319.4:c.77169C= (TTN)	NP_003310.4:p.Ser25723=
NM_133378.4:c.96660C= (TTN)	NP_596869.4:p.Ser32220=
NM_133432.3:c.77544C= (TTN)	NP_597676.3:p.Ser25848=
NM_133437.4:c.77745C= (TTN)	NP_597681.4:p.Ser25915=
NR_038271.1:n.446+8615G= (TTN-AS1)
NR_038272.1:n.220-3481G= (TTN-AS1)
XM_011511729.1:c.103461C= (TTN)	XP_011510031.1:p.Ser34487=
XM_011511730.1:c.77355C= (TTN)	XP_011510032.1:p.Ser25785=
XM_011511731.1:c.77214C= (TTN)	XP_011510033.1:p.Ser25738=
XM_017004819.1:c.103257C= (TTN)	XP_016860308.1:p.Ser34419=
XM_017004820.1:c.98655C= (TTN)	XP_016860309.1:p.Ser32885=
XM_017004821.1:c.98652C= (TTN)	XP_016860310.1:p.Ser32884=
XM_017004822.1:c.95694C= (TTN)	XP_016860311.1:p.Ser31898=
XM_017004823.1:c.77310C= (TTN)	XP_016860312.1:p.Ser25770=
XM_024453094.1:c.98805C= (TTN)	XP_024308862.1:p.Ser32935=
XM_024453095.1:c.98802C= (TTN)	XP_024308863.1:p.Ser32934=
XM_024453096.1:c.98235C= (TTN)	XP_024308864.1:p.Ser32745=
XM_024453097.1:c.95577C= (TTN)	XP_024308865.1:p.Ser31859=
XM_024453098.1:c.95496C= (TTN)	XP_024308866.1:p.Ser31832=
XM_024453099.1:c.77259C= (TTN)	XP_024308867.1:p.Ser25753=
XM_024453100.1:c.67113C= (TTN)	XP_024308868.1:p.Ser22371=