Canonical Allele Identifier: CA139946

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178605072C>T , CM000664.2:g.178605072C>T	GRCh38
NC_000002.11:g.179469799C>T , CM000664.1:g.179469799C>T	GRCh37
NC_000002.10:g.179178044C>T	NCBI36
NG_011618.3:g.230731G>A , LRG_391:g.230731G>A
NG_051363.1:g.87246C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.54105G>A (TTN) MANE Select	NP_001254479.2:p.Ala18035=
ENST00000589042.5:c.54105G>A (TTN) MANE Select	ENSP00000467141.1:p.Ala18035=
NM_001256850.1:c.49182G>A (TTN)	NP_001243779.1:p.Ala16394=
NM_003319.4:c.26910G>A (TTN)	NP_003310.4:p.Ala8970=
NM_133378.4:c.46401G>A (TTN)	NP_596869.4:p.Ala15467=
NM_133432.3:c.27285G>A (TTN)	NP_597676.3:p.Ala9095=
NM_133437.4:c.27486G>A (TTN)	NP_597681.4:p.Ala9162=
NR_038271.1:n.683-3095C>T (TTN-AS1)
NR_038272.1:n.4259C>T (TTN-AS1)
ENST00000342175.10:c.27486G>A (TTN)	ENSP00000340554.6:p.Ala9162=
ENST00000342175.11:c.27486G>A (TTN)	ENSP00000340554.6:p.Ala9162=
ENST00000342992.10:c.46401G>A (TTN)	ENSP00000343764.6:p.Ala15467=
ENST00000342992.11:c.46401G>A (TTN)	ENSP00000343764.6:p.Ala15467=
ENST00000359218.10:c.27285G>A (TTN)	ENSP00000352154.5:p.Ala9095=
ENST00000359218.9:c.27285G>A (TTN)	ENSP00000352154.5:p.Ala9095=
ENST00000460472.6:c.26910G>A (TTN)	ENSP00000434586.1:p.Ala8970=
ENST00000591111.5:c.49182G>A (TTN)	ENSP00000465570.1:p.Ala16394=
ENST00000615779.4:c.49182G>A (TTN)	ENSP00000483597.1:p.Ala16394=
XM_011511729.1:c.53202G>A (TTN)	XP_011510031.1:p.Ala17734=
XM_011511730.1:c.27096G>A (TTN)	XP_011510032.1:p.Ala9032=
XM_011511731.1:c.26955G>A (TTN)	XP_011510033.1:p.Ala8985=
XM_017004819.1:c.52998G>A (TTN)	XP_016860308.1:p.Ala17666=
XM_017004820.1:c.48396G>A (TTN)	XP_016860309.1:p.Ala16132=
XM_017004821.1:c.48393G>A (TTN)	XP_016860310.1:p.Ala16131=
XM_017004822.1:c.45435G>A (TTN)	XP_016860311.1:p.Ala15145=
XM_017004823.1:c.27051G>A (TTN)	XP_016860312.1:p.Ala9017=
XM_024453094.1:c.48546G>A (TTN)	XP_024308862.1:p.Ala16182=
XM_024453095.1:c.48543G>A (TTN)	XP_024308863.1:p.Ala16181=
XM_024453096.1:c.47976G>A (TTN)	XP_024308864.1:p.Ala15992=
XM_024453097.1:c.45318G>A (TTN)	XP_024308865.1:p.Ala15106=
XM_024453098.1:c.45237G>A (TTN)	XP_024308866.1:p.Ala15079=
XM_024453099.1:c.27000G>A (TTN)	XP_024308867.1:p.Ala9000=
XM_024453100.1:c.16854G>A (TTN)	XP_024308868.1:p.Ala5618=