Canonical Allele Identifier: CA1310546584

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178607495G= , CM000664.2:g.178607495G=	GRCh38
NC_000002.11:g.179472222G= , CM000664.1:g.179472222G=	GRCh37
NC_000002.10:g.179180467G=	NCBI36
NG_011618.3:g.228308C= , LRG_391:g.228308C=
NG_051363.1:g.89669G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.45489C= (TTN)	ENSP00000343764.6:p.Ile15163=
ENST00000342175.11:c.26574C= (TTN)	ENSP00000340554.6:p.Ile8858=
ENST00000359218.10:c.26373C= (TTN)	ENSP00000352154.5:p.Ile8791=
ENST00000342175.10:c.26574C= (TTN)	ENSP00000340554.6:p.Ile8858=
ENST00000342992.10:c.45489C= (TTN)	ENSP00000343764.6:p.Ile15163=
ENST00000359218.9:c.26373C= (TTN)	ENSP00000352154.5:p.Ile8791=
ENST00000460472.6:c.25998C= (TTN)	ENSP00000434586.1:p.Ile8666=
ENST00000589042.5:c.53193C= (TTN) MANE Select	ENSP00000467141.1:p.Ile17731=
ENST00000591111.5:c.48270C= (TTN)	ENSP00000465570.1:p.Ile16090=
ENST00000615779.4:c.48270C= (TTN)	ENSP00000483597.1:p.Ile16090=
NM_001256850.1:c.48270C= (TTN)	NP_001243779.1:p.Ile16090=
NM_001267550.2:c.53193C= (TTN) MANE Select	NP_001254479.2:p.Ile17731=
NM_003319.4:c.25998C= (TTN)	NP_003310.4:p.Ile8666=
NM_133378.4:c.45489C= (TTN)	NP_596869.4:p.Ile15163=
NM_133432.3:c.26373C= (TTN)	NP_597676.3:p.Ile8791=
NM_133437.4:c.26574C= (TTN)	NP_597681.4:p.Ile8858=
NR_038271.1:n.683-672G= (TTN-AS1)
XM_011511729.1:c.52290C= (TTN)	XP_011510031.1:p.Ile17430=
XM_011511730.1:c.26184C= (TTN)	XP_011510032.1:p.Ile8728=
XM_011511731.1:c.26043C= (TTN)	XP_011510033.1:p.Ile8681=
XM_017004819.1:c.52086C= (TTN)	XP_016860308.1:p.Ile17362=
XM_017004820.1:c.47484C= (TTN)	XP_016860309.1:p.Ile15828=
XM_017004821.1:c.47481C= (TTN)	XP_016860310.1:p.Ile15827=
XM_017004822.1:c.44523C= (TTN)	XP_016860311.1:p.Ile14841=
XM_017004823.1:c.26139C= (TTN)	XP_016860312.1:p.Ile8713=
XM_024453094.1:c.47634C= (TTN)	XP_024308862.1:p.Ile15878=
XM_024453095.1:c.47631C= (TTN)	XP_024308863.1:p.Ile15877=
XM_024453096.1:c.47064C= (TTN)	XP_024308864.1:p.Ile15688=
XM_024453097.1:c.44406C= (TTN)	XP_024308865.1:p.Ile14802=
XM_024453098.1:c.44325C= (TTN)	XP_024308866.1:p.Ile14775=
XM_024453099.1:c.26088C= (TTN)	XP_024308867.1:p.Ile8696=
XM_024453100.1:c.15942C= (TTN)	XP_024308868.1:p.Ile5314=