Canonical Allele Identifier: CA1310518133

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178532229_178532232delinsCCTT , CM000664.2:g.178532229_178532232delinsCCTT GRCh38
NC_000002.11:g.179396956_179396959delinsCCTT , CM000664.1:g.179396956_179396959delinsCCTT GRCh37
NC_000002.10:g.179105202_179105205delinsCCTT NCBI36
NG_011618.3:g.303571_303574delinsAAGG , LRG_391:g.303571_303574delinsAAGG
NG_051363.1:g.14403_14406delinsCCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.96679_96682delinsAAGG (TTN) ENSP00000343764.6:p.Lys32227=
ENST00000342175.11:c.77764_77767delinsAAGG (TTN) ENSP00000340554.6:p.Lys25922=
ENST00000359218.10:c.77563_77566delinsAAGG (TTN) ENSP00000352154.5:p.Lys25855=
ENST00000342175.10:c.77764_77767delinsAAGG (TTN) ENSP00000340554.6:p.Lys25922=
ENST00000342992.10:c.96679_96682delinsAAGG (TTN) ENSP00000343764.6:p.Lys32227=
ENST00000359218.9:c.77563_77566delinsAAGG (TTN) ENSP00000352154.5:p.Lys25855=
ENST00000460472.6:c.77188_77191delinsAAGG (TTN) ENSP00000434586.1:p.Lys25730=
ENST00000589042.5:c.104383_104386delinsAAGG (TTN) MANE Select ENSP00000467141.1:p.Lys34795=
ENST00000591111.5:c.99460_99463delinsAAGG (TTN) ENSP00000465570.1:p.Lys33154=
ENST00000615779.4:c.99460_99463delinsAAGG (TTN) ENSP00000483597.1:p.Lys33154=
NM_001256850.1:c.99460_99463delinsAAGG (TTN) NP_001243779.1:p.Lys33154=
NM_001267550.2:c.104383_104386delinsAAGG (TTN) MANE Select NP_001254479.2:p.Lys34795=
NM_003319.4:c.77188_77191delinsAAGG (TTN) NP_003310.4:p.Lys25730=
NM_133378.4:c.96679_96682delinsAAGG (TTN) NP_596869.4:p.Lys32227=
NM_133432.3:c.77563_77566delinsAAGG (TTN) NP_597676.3:p.Lys25855=
NM_133437.4:c.77764_77767delinsAAGG (TTN) NP_597681.4:p.Lys25922=
NR_038271.1:n.446+8593_446+8596delinsCCTT (TTN-AS1)
NR_038272.1:n.220-3503_220-3500delinsCCTT (TTN-AS1)
XM_011511729.1:c.103480_103483delinsAAGG (TTN) XP_011510031.1:p.Lys34494=
XM_011511730.1:c.77374_77377delinsAAGG (TTN) XP_011510032.1:p.Lys25792=
XM_011511731.1:c.77233_77236delinsAAGG (TTN) XP_011510033.1:p.Lys25745=
XM_017004819.1:c.103276_103279delinsAAGG (TTN) XP_016860308.1:p.Lys34426=
XM_017004820.1:c.98674_98677delinsAAGG (TTN) XP_016860309.1:p.Lys32892=
XM_017004821.1:c.98671_98674delinsAAGG (TTN) XP_016860310.1:p.Lys32891=
XM_017004822.1:c.95713_95716delinsAAGG (TTN) XP_016860311.1:p.Lys31905=
XM_017004823.1:c.77329_77332delinsAAGG (TTN) XP_016860312.1:p.Lys25777=
XM_024453094.1:c.98824_98827delinsAAGG (TTN) XP_024308862.1:p.Lys32942=
XM_024453095.1:c.98821_98824delinsAAGG (TTN) XP_024308863.1:p.Lys32941=
XM_024453096.1:c.98254_98257delinsAAGG (TTN) XP_024308864.1:p.Lys32752=
XM_024453097.1:c.95596_95599delinsAAGG (TTN) XP_024308865.1:p.Lys31866=
XM_024453098.1:c.95515_95518delinsAAGG (TTN) XP_024308866.1:p.Lys31839=
XM_024453099.1:c.77278_77281delinsAAGG (TTN) XP_024308867.1:p.Lys25760=
XM_024453100.1:c.67132_67135delinsAAGG (TTN) XP_024308868.1:p.Lys22378=