Canonical Allele Identifier: CA1310518045

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532042A= , CM000664.2:g.178532042A=	GRCh38
NC_000002.11:g.179396769A= , CM000664.1:g.179396769A=	GRCh37
NC_000002.10:g.179105015A=	NCBI36
NG_011618.3:g.303761T= , LRG_391:g.303761T=
NG_051363.1:g.14216A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96869T= (TTN)	ENSP00000343764.6:p.Ile32290=
ENST00000342175.11:c.77954T= (TTN)	ENSP00000340554.6:p.Ile25985=
ENST00000359218.10:c.77753T= (TTN)	ENSP00000352154.5:p.Ile25918=
ENST00000342175.10:c.77954T= (TTN)	ENSP00000340554.6:p.Ile25985=
ENST00000342992.10:c.96869T= (TTN)	ENSP00000343764.6:p.Ile32290=
ENST00000359218.9:c.77753T= (TTN)	ENSP00000352154.5:p.Ile25918=
ENST00000460472.6:c.77378T= (TTN)	ENSP00000434586.1:p.Ile25793=
ENST00000589042.5:c.104573T= (TTN) MANE Select	ENSP00000467141.1:p.Ile34858=
ENST00000591111.5:c.99650T= (TTN)	ENSP00000465570.1:p.Ile33217=
ENST00000615779.4:c.99650T= (TTN)	ENSP00000483597.1:p.Ile33217=
NM_001256850.1:c.99650T= (TTN)	NP_001243779.1:p.Ile33217=
NM_001267550.2:c.104573T= (TTN) MANE Select	NP_001254479.2:p.Ile34858=
NM_003319.4:c.77378T= (TTN)	NP_003310.4:p.Ile25793=
NM_133378.4:c.96869T= (TTN)	NP_596869.4:p.Ile32290=
NM_133432.3:c.77753T= (TTN)	NP_597676.3:p.Ile25918=
NM_133437.4:c.77954T= (TTN)	NP_597681.4:p.Ile25985=
NR_038271.1:n.446+8406A= (TTN-AS1)
NR_038272.1:n.220-3690A= (TTN-AS1)
XM_011511729.1:c.103670T= (TTN)	XP_011510031.1:p.Ile34557=
XM_011511730.1:c.77564T= (TTN)	XP_011510032.1:p.Ile25855=
XM_011511731.1:c.77423T= (TTN)	XP_011510033.1:p.Ile25808=
XM_017004819.1:c.103466T= (TTN)	XP_016860308.1:p.Ile34489=
XM_017004820.1:c.98864T= (TTN)	XP_016860309.1:p.Ile32955=
XM_017004821.1:c.98861T= (TTN)	XP_016860310.1:p.Ile32954=
XM_017004822.1:c.95903T= (TTN)	XP_016860311.1:p.Ile31968=
XM_017004823.1:c.77519T= (TTN)	XP_016860312.1:p.Ile25840=
XM_024453094.1:c.99014T= (TTN)	XP_024308862.1:p.Ile33005=
XM_024453095.1:c.99011T= (TTN)	XP_024308863.1:p.Ile33004=
XM_024453096.1:c.98444T= (TTN)	XP_024308864.1:p.Ile32815=
XM_024453097.1:c.95786T= (TTN)	XP_024308865.1:p.Ile31929=
XM_024453098.1:c.95705T= (TTN)	XP_024308866.1:p.Ile31902=
XM_024453099.1:c.77468T= (TTN)	XP_024308867.1:p.Ile25823=
XM_024453100.1:c.67322T= (TTN)	XP_024308868.1:p.Ile22441=