Canonical Allele Identifier: CA2662129163

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178570945-CAAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178570950_178570952del , CM000664.2:g.178570950_178570952del	GRCh38
NC_000002.11:g.179435677_179435679del , CM000664.1:g.179435677_179435679del	GRCh37
NC_000002.10:g.179143923_179143925del	NCBI36
NG_011618.3:g.264855_264857del , LRG_391:g.264855_264857del
NG_051363.1:g.53124_53126del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.67480_67482del (TTN)	ENSP00000343764.6:p.Ile22494del
ENST00000342175.11:c.48565_48567del (TTN)	ENSP00000340554.6:p.Ile16189del
ENST00000359218.10:c.48364_48366del (TTN)	ENSP00000352154.5:p.Ile16122del
ENST00000342175.10:c.48565_48567del (TTN)	ENSP00000340554.6:p.Ile16189del
ENST00000342992.10:c.67480_67482del (TTN)	ENSP00000343764.6:p.Ile22494del
ENST00000359218.9:c.48364_48366del (TTN)	ENSP00000352154.5:p.Ile16122del
ENST00000460472.6:c.47989_47991del (TTN)	ENSP00000434586.1:p.Ile15997del
ENST00000589042.5:c.75184_75186del (TTN) MANE Select	ENSP00000467141.1:p.Ile25062del
ENST00000591111.5:c.70261_70263del (TTN)	ENSP00000465570.1:p.Ile23421del
ENST00000615779.4:c.70261_70263del (TTN)	ENSP00000483597.1:p.Ile23421del
NM_001256850.1:c.70261_70263del (TTN)	NP_001243779.1:p.Ile23421del
NM_001267550.2:c.75184_75186del (TTN) MANE Select	NP_001254479.2:p.Ile25062del
NM_003319.4:c.47989_47991del (TTN)	NP_003310.4:p.Ile15997del
NM_133378.4:c.67480_67482del (TTN)	NP_596869.4:p.Ile22494del
NM_133432.3:c.48364_48366del (TTN)	NP_597676.3:p.Ile16122del
NM_133437.4:c.48565_48567del (TTN)	NP_597681.4:p.Ile16189del
NR_038271.1:n.447-350_447-348del (TTN-AS1)
NR_038272.1:n.2044-11622_2044-11620del (TTN-AS1)
XM_011511729.1:c.74281_74283del (TTN)	XP_011510031.1:p.Ile24761del
XM_011511730.1:c.48175_48177del (TTN)	XP_011510032.1:p.Ile16059del
XM_011511731.1:c.48034_48036del (TTN)	XP_011510033.1:p.Ile16012del
XM_017004819.1:c.74077_74079del (TTN)	XP_016860308.1:p.Ile24693del
XM_017004820.1:c.69475_69477del (TTN)	XP_016860309.1:p.Ile23159del
XM_017004821.1:c.69472_69474del (TTN)	XP_016860310.1:p.Ile23158del
XM_017004822.1:c.66514_66516del (TTN)	XP_016860311.1:p.Ile22172del
XM_017004823.1:c.48130_48132del (TTN)	XP_016860312.1:p.Ile16044del
XM_024453094.1:c.69625_69627del (TTN)	XP_024308862.1:p.Ile23209del
XM_024453095.1:c.69622_69624del (TTN)	XP_024308863.1:p.Ile23208del
XM_024453096.1:c.69055_69057del (TTN)	XP_024308864.1:p.Ile23019del
XM_024453097.1:c.66397_66399del (TTN)	XP_024308865.1:p.Ile22133del
XM_024453098.1:c.66316_66318del (TTN)	XP_024308866.1:p.Ile22106del
XM_024453099.1:c.48079_48081del (TTN)	XP_024308867.1:p.Ile16027del
XM_024453100.1:c.37933_37935del (TTN)	XP_024308868.1:p.Ile12645del