Canonical Allele Identifier: CA2825001004

Gene: TTN TTN-AS1

Linked Data

• ClinVar Variation Id: 3223359
• ClinVar RCV Id: RCV004508714

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532622_178532623delinsCC , CM000664.2:g.178532622_178532623delinsCC	GRCh38
NC_000002.11:g.179397349_179397350delinsCC , CM000664.1:g.179397349_179397350delinsCC	GRCh37
NC_000002.10:g.179105595_179105596delinsCC	NCBI36
NG_011618.3:g.303180_303181delinsGG , LRG_391:g.303180_303181delinsGG
NG_051363.1:g.14796_14797delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96288_96289delinsGG (TTN)	ENSP00000343764.6:p.Leu32097Val
ENST00000342175.11:c.77373_77374delinsGG (TTN)	ENSP00000340554.6:p.Leu25792Val
ENST00000359218.10:c.77172_77173delinsGG (TTN)	ENSP00000352154.5:p.Leu25725Val
ENST00000342175.10:c.77373_77374delinsGG (TTN)	ENSP00000340554.6:p.Leu25792Val
ENST00000342992.10:c.96288_96289delinsGG (TTN)	ENSP00000343764.6:p.Leu32097Val
ENST00000359218.9:c.77172_77173delinsGG (TTN)	ENSP00000352154.5:p.Leu25725Val
ENST00000460472.6:c.76797_76798delinsGG (TTN)	ENSP00000434586.1:p.Leu25600Val
ENST00000589042.5:c.103992_103993delinsGG (TTN) MANE Select	ENSP00000467141.1:p.Leu34665Val
ENST00000591111.5:c.99069_99070delinsGG (TTN)	ENSP00000465570.1:p.Leu33024Val
ENST00000615779.4:c.99069_99070delinsGG (TTN)	ENSP00000483597.1:p.Leu33024Val
NM_001256850.1:c.99069_99070delinsGG (TTN)	NP_001243779.1:p.Leu33024Val
NM_001267550.2:c.103992_103993delinsGG (TTN) MANE Select	NP_001254479.2:p.Leu34665Val
NM_003319.4:c.76797_76798delinsGG (TTN)	NP_003310.4:p.Leu25600Val
NM_133378.4:c.96288_96289delinsGG (TTN)	NP_596869.4:p.Leu32097Val
NM_133432.3:c.77172_77173delinsGG (TTN)	NP_597676.3:p.Leu25725Val
NM_133437.4:c.77373_77374delinsGG (TTN)	NP_597681.4:p.Leu25792Val
NR_038271.1:n.446+8986_446+8987delinsCC (TTN-AS1)
NR_038272.1:n.220-3110_220-3109delinsCC (TTN-AS1)
XM_011511729.1:c.103089_103090delinsGG (TTN)	XP_011510031.1:p.Leu34364Val
XM_011511730.1:c.76983_76984delinsGG (TTN)	XP_011510032.1:p.Leu25662Val
XM_011511731.1:c.76842_76843delinsGG (TTN)	XP_011510033.1:p.Leu25615Val
XM_017004819.1:c.102885_102886delinsGG (TTN)	XP_016860308.1:p.Leu34296Val
XM_017004820.1:c.98283_98284delinsGG (TTN)	XP_016860309.1:p.Leu32762Val
XM_017004821.1:c.98280_98281delinsGG (TTN)	XP_016860310.1:p.Leu32761Val
XM_017004822.1:c.95322_95323delinsGG (TTN)	XP_016860311.1:p.Leu31775Val
XM_017004823.1:c.76938_76939delinsGG (TTN)	XP_016860312.1:p.Leu25647Val
XM_024453094.1:c.98433_98434delinsGG (TTN)	XP_024308862.1:p.Leu32812Val
XM_024453095.1:c.98430_98431delinsGG (TTN)	XP_024308863.1:p.Leu32811Val
XM_024453096.1:c.97863_97864delinsGG (TTN)	XP_024308864.1:p.Leu32622Val
XM_024453097.1:c.95205_95206delinsGG (TTN)	XP_024308865.1:p.Leu31736Val
XM_024453098.1:c.95124_95125delinsGG (TTN)	XP_024308866.1:p.Leu31709Val
XM_024453099.1:c.76887_76888delinsGG (TTN)	XP_024308867.1:p.Leu25630Val
XM_024453100.1:c.66741_66742delinsGG (TTN)	XP_024308868.1:p.Leu22248Val