Canonical Allele Identifier: CA1310540468

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178591916_178591917delinsGA , CM000664.2:g.178591916_178591917delinsGA GRCh38
NC_000002.11:g.179456643_179456644delinsGA , CM000664.1:g.179456643_179456644delinsGA GRCh37
NC_000002.10:g.179164889_179164890delinsGA NCBI36
NG_011618.3:g.243886_243887delinsTC , LRG_391:g.243886_243887delinsTC
NG_051363.1:g.74090_74091delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.52223-25_52223-24delinsTC (TTN) ENSP00000343764.6:n.52223-25_52223-24delinsTC
ENST00000342175.11:c.33308-25_33308-24delinsTC (TTN) ENSP00000340554.6:n.33308-25_33308-24delinsTC
ENST00000359218.10:c.33107-25_33107-24delinsTC (TTN) ENSP00000352154.5:n.33107-25_33107-24delinsTC
ENST00000342175.10:c.33308-25_33308-24delinsTC (TTN) ENSP00000340554.6:n.33308-25_33308-24delinsTC
ENST00000342992.10:c.52223-25_52223-24delinsTC (TTN) ENSP00000343764.6:n.52223-25_52223-24delinsTC
ENST00000359218.9:c.33107-25_33107-24delinsTC (TTN) ENSP00000352154.5:n.33107-25_33107-24delinsTC
ENST00000460472.6:c.32732-25_32732-24delinsTC (TTN) ENSP00000434586.1:n.32732-25_32732-24delinsTC
ENST00000589042.5:c.59927-25_59927-24delinsTC (TTN) MANE Select ENSP00000467141.1:n.59927-25_59927-24delinsTC
ENST00000591111.5:c.55004-25_55004-24delinsTC (TTN) ENSP00000465570.1:n.55004-25_55004-24delinsTC
ENST00000615779.4:c.55004-25_55004-24delinsTC (TTN) ENSP00000483597.1:n.55004-25_55004-24delinsTC
NM_001256850.1:c.55004-25_55004-24delinsTC (TTN) NP_001243779.1:n.55004-25_55004-24delinsTC
NM_001267550.2:c.59927-25_59927-24delinsTC (TTN) MANE Select NP_001254479.2:n.59927-25_59927-24delinsTC
NM_003319.4:c.32732-25_32732-24delinsTC (TTN) NP_003310.4:n.32732-25_32732-24delinsTC
NM_133378.4:c.52223-25_52223-24delinsTC (TTN) NP_596869.4:n.52223-25_52223-24delinsTC
NM_133432.3:c.33107-25_33107-24delinsTC (TTN) NP_597676.3:n.33107-25_33107-24delinsTC
NM_133437.4:c.33308-25_33308-24delinsTC (TTN) NP_597681.4:n.33308-25_33308-24delinsTC
NR_038271.1:n.597-5680_597-5679delinsGA (TTN-AS1)
NR_038272.1:n.3364+602_3364+603delinsGA (TTN-AS1)
XM_011511729.1:c.59024-25_59024-24delinsTC (TTN) XP_011510031.1:n.59024-25_59024-24delinsTC
XM_011511730.1:c.32918-25_32918-24delinsTC (TTN) XP_011510032.1:n.32918-25_32918-24delinsTC
XM_011511731.1:c.32777-25_32777-24delinsTC (TTN) XP_011510033.1:n.32777-25_32777-24delinsTC
XM_017004819.1:c.58820-25_58820-24delinsTC (TTN) XP_016860308.1:n.58820-25_58820-24delinsTC
XM_017004820.1:c.54218-25_54218-24delinsTC (TTN) XP_016860309.1:n.54218-25_54218-24delinsTC
XM_017004821.1:c.54215-25_54215-24delinsTC (TTN) XP_016860310.1:n.54215-25_54215-24delinsTC
XM_017004822.1:c.51257-25_51257-24delinsTC (TTN) XP_016860311.1:n.51257-25_51257-24delinsTC
XM_017004823.1:c.32873-25_32873-24delinsTC (TTN) XP_016860312.1:n.32873-25_32873-24delinsTC
XM_024453094.1:c.54368-25_54368-24delinsTC (TTN) XP_024308862.1:n.54368-25_54368-24delinsTC
XM_024453095.1:c.54365-25_54365-24delinsTC (TTN) XP_024308863.1:n.54365-25_54365-24delinsTC
XM_024453096.1:c.53798-25_53798-24delinsTC (TTN) XP_024308864.1:n.53798-25_53798-24delinsTC
XM_024453097.1:c.51140-25_51140-24delinsTC (TTN) XP_024308865.1:n.51140-25_51140-24delinsTC
XM_024453098.1:c.51059-25_51059-24delinsTC (TTN) XP_024308866.1:n.51059-25_51059-24delinsTC
XM_024453099.1:c.32822-25_32822-24delinsTC (TTN) XP_024308867.1:n.32822-25_32822-24delinsTC
XM_024453100.1:c.22676-25_22676-24delinsTC (TTN) XP_024308868.1:n.22676-25_22676-24delinsTC