Canonical Allele Identifier: CA1310518081

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178532104_178532107delinsCAGT , CM000664.2:g.178532104_178532107delinsCAGT GRCh38
NC_000002.11:g.179396831_179396834delinsCAGT , CM000664.1:g.179396831_179396834delinsCAGT GRCh37
NC_000002.10:g.179105077_179105080delinsCAGT NCBI36
NG_011618.3:g.303696_303699delinsACTG , LRG_391:g.303696_303699delinsACTG
NG_051363.1:g.14278_14281delinsCAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.96804_96807delinsACTG (TTN) ENSP00000343764.6:p.Leu32268=
ENST00000342175.11:c.77889_77892delinsACTG (TTN) ENSP00000340554.6:p.Leu25963=
ENST00000359218.10:c.77688_77691delinsACTG (TTN) ENSP00000352154.5:p.Leu25896=
ENST00000342175.10:c.77889_77892delinsACTG (TTN) ENSP00000340554.6:p.Leu25963=
ENST00000342992.10:c.96804_96807delinsACTG (TTN) ENSP00000343764.6:p.Leu32268=
ENST00000359218.9:c.77688_77691delinsACTG (TTN) ENSP00000352154.5:p.Leu25896=
ENST00000460472.6:c.77313_77316delinsACTG (TTN) ENSP00000434586.1:p.Leu25771=
ENST00000589042.5:c.104508_104511delinsACTG (TTN) MANE Select ENSP00000467141.1:p.Leu34836=
ENST00000591111.5:c.99585_99588delinsACTG (TTN) ENSP00000465570.1:p.Leu33195=
ENST00000615779.4:c.99585_99588delinsACTG (TTN) ENSP00000483597.1:p.Leu33195=
NM_001256850.1:c.99585_99588delinsACTG (TTN) NP_001243779.1:p.Leu33195=
NM_001267550.2:c.104508_104511delinsACTG (TTN) MANE Select NP_001254479.2:p.Leu34836=
NM_003319.4:c.77313_77316delinsACTG (TTN) NP_003310.4:p.Leu25771=
NM_133378.4:c.96804_96807delinsACTG (TTN) NP_596869.4:p.Leu32268=
NM_133432.3:c.77688_77691delinsACTG (TTN) NP_597676.3:p.Leu25896=
NM_133437.4:c.77889_77892delinsACTG (TTN) NP_597681.4:p.Leu25963=
NR_038271.1:n.446+8468_446+8471delinsCAGT (TTN-AS1)
NR_038272.1:n.220-3628_220-3625delinsCAGT (TTN-AS1)
XM_011511729.1:c.103605_103608delinsACTG (TTN) XP_011510031.1:p.Leu34535=
XM_011511730.1:c.77499_77502delinsACTG (TTN) XP_011510032.1:p.Leu25833=
XM_011511731.1:c.77358_77361delinsACTG (TTN) XP_011510033.1:p.Leu25786=
XM_017004819.1:c.103401_103404delinsACTG (TTN) XP_016860308.1:p.Leu34467=
XM_017004820.1:c.98799_98802delinsACTG (TTN) XP_016860309.1:p.Leu32933=
XM_017004821.1:c.98796_98799delinsACTG (TTN) XP_016860310.1:p.Leu32932=
XM_017004822.1:c.95838_95841delinsACTG (TTN) XP_016860311.1:p.Leu31946=
XM_017004823.1:c.77454_77457delinsACTG (TTN) XP_016860312.1:p.Leu25818=
XM_024453094.1:c.98949_98952delinsACTG (TTN) XP_024308862.1:p.Leu32983=
XM_024453095.1:c.98946_98949delinsACTG (TTN) XP_024308863.1:p.Leu32982=
XM_024453096.1:c.98379_98382delinsACTG (TTN) XP_024308864.1:p.Leu32793=
XM_024453097.1:c.95721_95724delinsACTG (TTN) XP_024308865.1:p.Leu31907=
XM_024453098.1:c.95640_95643delinsACTG (TTN) XP_024308866.1:p.Leu31880=
XM_024453099.1:c.77403_77406delinsACTG (TTN) XP_024308867.1:p.Leu25801=
XM_024453100.1:c.67257_67260delinsACTG (TTN) XP_024308868.1:p.Leu22419=