Canonical Allele Identifier: CA1310546581

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178607482G= , CM000664.2:g.178607482G=	GRCh38
NC_000002.11:g.179472209G= , CM000664.1:g.179472209G=	GRCh37
NC_000002.10:g.179180454G=	NCBI36
NG_011618.3:g.228321C= , LRG_391:g.228321C=
NG_051363.1:g.89656G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.45502C= (TTN)	ENSP00000343764.6:p.Arg15168=
ENST00000342175.11:c.26587C= (TTN)	ENSP00000340554.6:p.Arg8863=
ENST00000359218.10:c.26386C= (TTN)	ENSP00000352154.5:p.Arg8796=
ENST00000342175.10:c.26587C= (TTN)	ENSP00000340554.6:p.Arg8863=
ENST00000342992.10:c.45502C= (TTN)	ENSP00000343764.6:p.Arg15168=
ENST00000359218.9:c.26386C= (TTN)	ENSP00000352154.5:p.Arg8796=
ENST00000460472.6:c.26011C= (TTN)	ENSP00000434586.1:p.Arg8671=
ENST00000589042.5:c.53206C= (TTN) MANE Select	ENSP00000467141.1:p.Arg17736=
ENST00000591111.5:c.48283C= (TTN)	ENSP00000465570.1:p.Arg16095=
ENST00000615779.4:c.48283C= (TTN)	ENSP00000483597.1:p.Arg16095=
NM_001256850.1:c.48283C= (TTN)	NP_001243779.1:p.Arg16095=
NM_001267550.2:c.53206C= (TTN) MANE Select	NP_001254479.2:p.Arg17736=
NM_003319.4:c.26011C= (TTN)	NP_003310.4:p.Arg8671=
NM_133378.4:c.45502C= (TTN)	NP_596869.4:p.Arg15168=
NM_133432.3:c.26386C= (TTN)	NP_597676.3:p.Arg8796=
NM_133437.4:c.26587C= (TTN)	NP_597681.4:p.Arg8863=
NR_038271.1:n.683-685G= (TTN-AS1)
XM_011511729.1:c.52303C= (TTN)	XP_011510031.1:p.Arg17435=
XM_011511730.1:c.26197C= (TTN)	XP_011510032.1:p.Arg8733=
XM_011511731.1:c.26056C= (TTN)	XP_011510033.1:p.Arg8686=
XM_017004819.1:c.52099C= (TTN)	XP_016860308.1:p.Arg17367=
XM_017004820.1:c.47497C= (TTN)	XP_016860309.1:p.Arg15833=
XM_017004821.1:c.47494C= (TTN)	XP_016860310.1:p.Arg15832=
XM_017004822.1:c.44536C= (TTN)	XP_016860311.1:p.Arg14846=
XM_017004823.1:c.26152C= (TTN)	XP_016860312.1:p.Arg8718=
XM_024453094.1:c.47647C= (TTN)	XP_024308862.1:p.Arg15883=
XM_024453095.1:c.47644C= (TTN)	XP_024308863.1:p.Arg15882=
XM_024453096.1:c.47077C= (TTN)	XP_024308864.1:p.Arg15693=
XM_024453097.1:c.44419C= (TTN)	XP_024308865.1:p.Arg14807=
XM_024453098.1:c.44338C= (TTN)	XP_024308866.1:p.Arg14780=
XM_024453099.1:c.26101C= (TTN)	XP_024308867.1:p.Arg8701=
XM_024453100.1:c.15955C= (TTN)	XP_024308868.1:p.Arg5319=