Canonical Allele Identifier: CA1310511457

Gene: TTN TTN-AS1

Linked Data

• dbSNP Id: rs1688387542

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530083_178530084insCA , CM000664.2:g.178530083_178530084insCA	GRCh38
NC_000002.11:g.179394810_179394811insCA , CM000664.1:g.179394810_179394811insCA	GRCh37
NC_000002.10:g.179103056_179103057insCA	NCBI36
NG_011618.3:g.305719_305720insTG , LRG_391:g.305719_305720insTG
NG_051363.1:g.12257_12258insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98703_98704insTG (TTN)	ENSP00000343764.6:p.Glu32902TrpfsTer9
ENST00000342175.11:c.79788_79789insTG (TTN)	ENSP00000340554.6:p.Glu26597TrpfsTer9
ENST00000359218.10:c.79587_79588insTG (TTN)	ENSP00000352154.5:p.Glu26530TrpfsTer9
ENST00000342175.10:c.79788_79789insTG (TTN)	ENSP00000340554.6:p.Glu26597TrpfsTer9
ENST00000342992.10:c.98703_98704insTG (TTN)	ENSP00000343764.6:p.Glu32902TrpfsTer9
ENST00000359218.9:c.79587_79588insTG (TTN)	ENSP00000352154.5:p.Glu26530TrpfsTer9
ENST00000460472.6:c.79212_79213insTG (TTN)	ENSP00000434586.1:p.Glu26405TrpfsTer9
ENST00000589042.5:c.106407_106408insTG (TTN) MANE Select	ENSP00000467141.1:p.Glu35470TrpfsTer9
ENST00000591111.5:c.101484_101485insTG (TTN)	ENSP00000465570.1:p.Glu33829TrpfsTer9
ENST00000615779.4:c.101484_101485insTG (TTN)	ENSP00000483597.1:p.Glu33829TrpfsTer9
NM_001256850.1:c.101484_101485insTG (TTN)	NP_001243779.1:p.Glu33829TrpfsTer9
NM_001267550.2:c.106407_106408insTG (TTN) MANE Select	NP_001254479.2:p.Glu35470TrpfsTer9
NM_003319.4:c.79212_79213insTG (TTN)	NP_003310.4:p.Glu26405TrpfsTer9
NM_133378.4:c.98703_98704insTG (TTN)	NP_596869.4:p.Glu32902TrpfsTer9
NM_133432.3:c.79587_79588insTG (TTN)	NP_597676.3:p.Glu26530TrpfsTer9
NM_133437.4:c.79788_79789insTG (TTN)	NP_597681.4:p.Glu26597TrpfsTer9
NR_038271.1:n.446+6447_446+6448insCA (TTN-AS1)
NR_038272.1:n.220-5649_220-5648insCA (TTN-AS1)
XM_011511729.1:c.105504_105505insTG (TTN)	XP_011510031.1:p.Glu35169TrpfsTer9
XM_011511730.1:c.79398_79399insTG (TTN)	XP_011510032.1:p.Glu26467TrpfsTer9
XM_011511731.1:c.79257_79258insTG (TTN)	XP_011510033.1:p.Glu26420TrpfsTer9
XM_017004819.1:c.105300_105301insTG (TTN)	XP_016860308.1:p.Glu35101TrpfsTer9
XM_017004820.1:c.100698_100699insTG (TTN)	XP_016860309.1:p.Glu33567TrpfsTer9
XM_017004821.1:c.100695_100696insTG (TTN)	XP_016860310.1:p.Glu33566TrpfsTer9
XM_017004822.1:c.97737_97738insTG (TTN)	XP_016860311.1:p.Glu32580TrpfsTer9
XM_017004823.1:c.79353_79354insTG (TTN)	XP_016860312.1:p.Glu26452TrpfsTer9
XM_024453094.1:c.100848_100849insTG (TTN)	XP_024308862.1:p.Glu33617TrpfsTer9
XM_024453095.1:c.100845_100846insTG (TTN)	XP_024308863.1:p.Glu33616TrpfsTer9
XM_024453096.1:c.100278_100279insTG (TTN)	XP_024308864.1:p.Glu33427TrpfsTer9
XM_024453097.1:c.97620_97621insTG (TTN)	XP_024308865.1:p.Glu32541TrpfsTer9
XM_024453098.1:c.97539_97540insTG (TTN)	XP_024308866.1:p.Glu32514TrpfsTer9
XM_024453099.1:c.79302_79303insTG (TTN)	XP_024308867.1:p.Glu26435TrpfsTer9
XM_024453100.1:c.69156_69157insTG (TTN)	XP_024308868.1:p.Glu23053TrpfsTer9