Canonical Allele Identifier: CA2586965337

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178573871del , CM000664.2:g.178573871del	GRCh38
NC_000002.11:g.179438598del , CM000664.1:g.179438598del	GRCh37
NC_000002.10:g.179146844del	NCBI36
NG_011618.3:g.261933del , LRG_391:g.261933del
NG_051363.1:g.56045del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.64558del (TTN)	ENSP00000343764.6:p.Val21520Ter
ENST00000342175.11:c.45643del (TTN)	ENSP00000340554.6:p.Val15215Ter
ENST00000359218.10:c.45442del (TTN)	ENSP00000352154.5:p.Val15148Ter
ENST00000342175.10:c.45643del (TTN)	ENSP00000340554.6:p.Val15215Ter
ENST00000342992.10:c.64558del (TTN)	ENSP00000343764.6:p.Val21520Ter
ENST00000359218.9:c.45442del (TTN)	ENSP00000352154.5:p.Val15148Ter
ENST00000460472.6:c.45067del (TTN)	ENSP00000434586.1:p.Val15023Ter
ENST00000589042.5:c.72262del (TTN) MANE Select	ENSP00000467141.1:p.Val24088Ter
ENST00000591111.5:c.67339del (TTN)	ENSP00000465570.1:p.Val22447Ter
ENST00000615779.4:c.67339del (TTN)	ENSP00000483597.1:p.Val22447Ter
NM_001256850.1:c.67339del (TTN)	NP_001243779.1:p.Val22447Ter
NM_001267550.2:c.72262del (TTN) MANE Select	NP_001254479.2:p.Val24088Ter
NM_003319.4:c.45067del (TTN)	NP_003310.4:p.Val15023Ter
NM_133378.4:c.64558del (TTN)	NP_596869.4:p.Val21520Ter
NM_133432.3:c.45442del (TTN)	NP_597676.3:p.Val15148Ter
NM_133437.4:c.45643del (TTN)	NP_597681.4:p.Val15215Ter
NR_038271.1:n.596+2422del (TTN-AS1)
NR_038272.1:n.2044-8701del (TTN-AS1)
XM_011511729.1:c.71359del (TTN)	XP_011510031.1:p.Val23787Ter
XM_011511730.1:c.45253del (TTN)	XP_011510032.1:p.Val15085Ter
XM_011511731.1:c.45112del (TTN)	XP_011510033.1:p.Val15038Ter
XM_017004819.1:c.71155del (TTN)	XP_016860308.1:p.Val23719Ter
XM_017004820.1:c.66553del (TTN)	XP_016860309.1:p.Val22185Ter
XM_017004821.1:c.66550del (TTN)	XP_016860310.1:p.Val22184Ter
XM_017004822.1:c.63592del (TTN)	XP_016860311.1:p.Val21198Ter
XM_017004823.1:c.45208del (TTN)	XP_016860312.1:p.Val15070Ter
XM_024453094.1:c.66703del (TTN)	XP_024308862.1:p.Val22235Ter
XM_024453095.1:c.66700del (TTN)	XP_024308863.1:p.Val22234Ter
XM_024453096.1:c.66133del (TTN)	XP_024308864.1:p.Val22045Ter
XM_024453097.1:c.63475del (TTN)	XP_024308865.1:p.Val21159Ter
XM_024453098.1:c.63394del (TTN)	XP_024308866.1:p.Val21132Ter
XM_024453099.1:c.45157del (TTN)	XP_024308867.1:p.Val15053Ter
XM_024453100.1:c.35011del (TTN)	XP_024308868.1:p.Val11671Ter