Canonical Allele Identifier: CA2662121293

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178537625-CGGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178537627_178537629del , CM000664.2:g.178537627_178537629del	GRCh38
NC_000002.11:g.179402354_179402356del , CM000664.1:g.179402354_179402356del	GRCh37
NC_000002.10:g.179110600_179110602del	NCBI36
NG_011618.3:g.298175_298177del , LRG_391:g.298175_298177del
NG_051363.1:g.19801_19803del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.91875_91877del (TTN)	ENSP00000343764.6:p.Pro30626del
ENST00000342175.11:c.72960_72962del (TTN)	ENSP00000340554.6:p.Pro24321del
ENST00000359218.10:c.72759_72761del (TTN)	ENSP00000352154.5:p.Pro24254del
ENST00000342175.10:c.72960_72962del (TTN)	ENSP00000340554.6:p.Pro24321del
ENST00000342992.10:c.91875_91877del (TTN)	ENSP00000343764.6:p.Pro30626del
ENST00000359218.9:c.72759_72761del (TTN)	ENSP00000352154.5:p.Pro24254del
ENST00000460472.6:c.72384_72386del (TTN)	ENSP00000434586.1:p.Pro24129del
ENST00000589042.5:c.99579_99581del (TTN) MANE Select	ENSP00000467141.1:p.Pro33194del
ENST00000591111.5:c.94656_94658del (TTN)	ENSP00000465570.1:p.Pro31553del
ENST00000615779.4:c.94656_94658del (TTN)	ENSP00000483597.1:p.Pro31553del
NM_001256850.1:c.94656_94658del (TTN)	NP_001243779.1:p.Pro31553del
NM_001267550.2:c.99579_99581del (TTN) MANE Select	NP_001254479.2:p.Pro33194del
NM_003319.4:c.72384_72386del (TTN)	NP_003310.4:p.Pro24129del
NM_133378.4:c.91875_91877del (TTN)	NP_596869.4:p.Pro30626del
NM_133432.3:c.72759_72761del (TTN)	NP_597676.3:p.Pro24254del
NM_133437.4:c.72960_72962del (TTN)	NP_597681.4:p.Pro24321del
NR_038271.1:n.446+13991_446+13993del (TTN-AS1)
NR_038272.1:n.583_585del (TTN-AS1)
XM_011511729.1:c.98676_98678del (TTN)	XP_011510031.1:p.Pro32893del
XM_011511730.1:c.72570_72572del (TTN)	XP_011510032.1:p.Pro24191del
XM_011511731.1:c.72429_72431del (TTN)	XP_011510033.1:p.Pro24144del
XM_017004819.1:c.98472_98474del (TTN)	XP_016860308.1:p.Pro32825del
XM_017004820.1:c.93870_93872del (TTN)	XP_016860309.1:p.Pro31291del
XM_017004821.1:c.93867_93869del (TTN)	XP_016860310.1:p.Pro31290del
XM_017004822.1:c.90909_90911del (TTN)	XP_016860311.1:p.Pro30304del
XM_017004823.1:c.72525_72527del (TTN)	XP_016860312.1:p.Pro24176del
XM_024453094.1:c.94020_94022del (TTN)	XP_024308862.1:p.Pro31341del
XM_024453095.1:c.94017_94019del (TTN)	XP_024308863.1:p.Pro31340del
XM_024453096.1:c.93450_93452del (TTN)	XP_024308864.1:p.Pro31151del
XM_024453097.1:c.90792_90794del (TTN)	XP_024308865.1:p.Pro30265del
XM_024453098.1:c.90711_90713del (TTN)	XP_024308866.1:p.Pro30238del
XM_024453099.1:c.72474_72476del (TTN)	XP_024308867.1:p.Pro24159del
XM_024453100.1:c.62328_62330del (TTN)	XP_024308868.1:p.Pro20777del