Canonical Allele Identifier: CA2662128507

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178559838-ATCAAGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178559841_178559846del , CM000664.2:g.178559841_178559846del	GRCh38
NC_000002.11:g.179424568_179424573del , CM000664.1:g.179424568_179424573del	GRCh37
NC_000002.10:g.179132814_179132819del	NCBI36
NG_011618.3:g.275959_275964del , LRG_391:g.275959_275964del
NG_051363.1:g.42015_42020del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.78584_78589del (TTN)	ENSP00000343764.6:p.Thr26195_Leu26196del
ENST00000342175.11:c.59669_59674del (TTN)	ENSP00000340554.6:p.Thr19890_Leu19891del
ENST00000359218.10:c.59468_59473del (TTN)	ENSP00000352154.5:p.Thr19823_Leu19824del
ENST00000342175.10:c.59669_59674del (TTN)	ENSP00000340554.6:p.Thr19890_Leu19891del
ENST00000342992.10:c.78584_78589del (TTN)	ENSP00000343764.6:p.Thr26195_Leu26196del
ENST00000359218.9:c.59468_59473del (TTN)	ENSP00000352154.5:p.Thr19823_Leu19824del
ENST00000460472.6:c.59093_59098del (TTN)	ENSP00000434586.1:p.Thr19698_Leu19699del
ENST00000589042.5:c.86288_86293del (TTN) MANE Select	ENSP00000467141.1:p.Thr28763_Leu28764del
ENST00000591111.5:c.81365_81370del (TTN)	ENSP00000465570.1:p.Thr27122_Leu27123del
ENST00000615779.4:c.81365_81370del (TTN)	ENSP00000483597.1:p.Thr27122_Leu27123del
NM_001256850.1:c.81365_81370del (TTN)	NP_001243779.1:p.Thr27122_Leu27123del
NM_001267550.2:c.86288_86293del (TTN) MANE Select	NP_001254479.2:p.Thr28763_Leu28764del
NM_003319.4:c.59093_59098del (TTN)	NP_003310.4:p.Thr19698_Leu19699del
NM_133378.4:c.78584_78589del (TTN)	NP_596869.4:p.Thr26195_Leu26196del
NM_133432.3:c.59468_59473del (TTN)	NP_597676.3:p.Thr19823_Leu19824del
NM_133437.4:c.59669_59674del (TTN)	NP_597681.4:p.Thr19890_Leu19891del
NR_038271.1:n.447-11459_447-11454del (TTN-AS1)
NR_038272.1:n.2043+17480_2043+17485del (TTN-AS1)
XM_011511729.1:c.85385_85390del (TTN)	XP_011510031.1:p.Thr28462_Leu28463del
XM_011511730.1:c.59279_59284del (TTN)	XP_011510032.1:p.Thr19760_Leu19761del
XM_011511731.1:c.59138_59143del (TTN)	XP_011510033.1:p.Thr19713_Leu19714del
XM_017004819.1:c.85181_85186del (TTN)	XP_016860308.1:p.Thr28394_Leu28395del
XM_017004820.1:c.80579_80584del (TTN)	XP_016860309.1:p.Thr26860_Leu26861del
XM_017004821.1:c.80576_80581del (TTN)	XP_016860310.1:p.Thr26859_Leu26860del
XM_017004822.1:c.77618_77623del (TTN)	XP_016860311.1:p.Thr25873_Leu25874del
XM_017004823.1:c.59234_59239del (TTN)	XP_016860312.1:p.Thr19745_Leu19746del
XM_024453094.1:c.80729_80734del (TTN)	XP_024308862.1:p.Thr26910_Leu26911del
XM_024453095.1:c.80726_80731del (TTN)	XP_024308863.1:p.Thr26909_Leu26910del
XM_024453096.1:c.80159_80164del (TTN)	XP_024308864.1:p.Thr26720_Leu26721del
XM_024453097.1:c.77501_77506del (TTN)	XP_024308865.1:p.Thr25834_Leu25835del
XM_024453098.1:c.77420_77425del (TTN)	XP_024308866.1:p.Thr25807_Leu25808del
XM_024453099.1:c.59183_59188del (TTN)	XP_024308867.1:p.Thr19728_Leu19729del
XM_024453100.1:c.49037_49042del (TTN)	XP_024308868.1:p.Thr16346_Leu16347del