Canonical Allele Identifier: CA1310520118

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178549812A= , CM000664.2:g.178549812A=	GRCh38
NC_000002.11:g.179414539A= , CM000664.1:g.179414539A=	GRCh37
NC_000002.10:g.179122785A=	NCBI36
NG_011618.3:g.285991T= , LRG_391:g.285991T=
NG_051363.1:g.31986A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.84206T= (TTN)	ENSP00000343764.6:p.Met28069=
ENST00000342175.11:c.65291T= (TTN)	ENSP00000340554.6:p.Met21764=
ENST00000359218.10:c.65090T= (TTN)	ENSP00000352154.5:p.Met21697=
ENST00000342175.10:c.65291T= (TTN)	ENSP00000340554.6:p.Met21764=
ENST00000342992.10:c.84206T= (TTN)	ENSP00000343764.6:p.Met28069=
ENST00000359218.9:c.65090T= (TTN)	ENSP00000352154.5:p.Met21697=
ENST00000460472.6:c.64715T= (TTN)	ENSP00000434586.1:p.Met21572=
ENST00000589042.5:c.91910T= (TTN) MANE Select	ENSP00000467141.1:p.Met30637=
ENST00000591111.5:c.86987T= (TTN)	ENSP00000465570.1:p.Met28996=
ENST00000615779.4:c.86987T= (TTN)	ENSP00000483597.1:p.Met28996=
NM_001256850.1:c.86987T= (TTN)	NP_001243779.1:p.Met28996=
NM_001267550.2:c.91910T= (TTN) MANE Select	NP_001254479.2:p.Met30637=
NM_003319.4:c.64715T= (TTN)	NP_003310.4:p.Met21572=
NM_133378.4:c.84206T= (TTN)	NP_596869.4:p.Met28069=
NM_133432.3:c.65090T= (TTN)	NP_597676.3:p.Met21697=
NM_133437.4:c.65291T= (TTN)	NP_597681.4:p.Met21764=
NR_038271.1:n.447-21488A= (TTN-AS1)
NR_038272.1:n.2043+7451A= (TTN-AS1)
XM_011511729.1:c.91007T= (TTN)	XP_011510031.1:p.Met30336=
XM_011511730.1:c.64901T= (TTN)	XP_011510032.1:p.Met21634=
XM_011511731.1:c.64760T= (TTN)	XP_011510033.1:p.Met21587=
XM_017004819.1:c.90803T= (TTN)	XP_016860308.1:p.Met30268=
XM_017004820.1:c.86201T= (TTN)	XP_016860309.1:p.Met28734=
XM_017004821.1:c.86198T= (TTN)	XP_016860310.1:p.Met28733=
XM_017004822.1:c.83240T= (TTN)	XP_016860311.1:p.Met27747=
XM_017004823.1:c.64856T= (TTN)	XP_016860312.1:p.Met21619=
XM_024453094.1:c.86351T= (TTN)	XP_024308862.1:p.Met28784=
XM_024453095.1:c.86348T= (TTN)	XP_024308863.1:p.Met28783=
XM_024453096.1:c.85781T= (TTN)	XP_024308864.1:p.Met28594=
XM_024453097.1:c.83123T= (TTN)	XP_024308865.1:p.Met27708=
XM_024453098.1:c.83042T= (TTN)	XP_024308866.1:p.Met27681=
XM_024453099.1:c.64805T= (TTN)	XP_024308867.1:p.Met21602=
XM_024453100.1:c.54659T= (TTN)	XP_024308868.1:p.Met18220=