Canonical Allele Identifier: CA1310522847

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178546215G= , CM000664.2:g.178546215G= GRCh38
NC_000002.11:g.179410942G= , CM000664.1:g.179410942G= GRCh37
NC_000002.10:g.179119188G= NCBI36
NG_011618.3:g.289588C= , LRG_391:g.289588C=
NG_051363.1:g.28389G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.87412C= (TTN) ENSP00000343764.6:p.Leu29138=
ENST00000342175.11:c.68497C= (TTN) ENSP00000340554.6:p.Leu22833=
ENST00000359218.10:c.68296C= (TTN) ENSP00000352154.5:p.Leu22766=
ENST00000342175.10:c.68497C= (TTN) ENSP00000340554.6:p.Leu22833=
ENST00000342992.10:c.87412C= (TTN) ENSP00000343764.6:p.Leu29138=
ENST00000359218.9:c.68296C= (TTN) ENSP00000352154.5:p.Leu22766=
ENST00000460472.6:c.67921C= (TTN) ENSP00000434586.1:p.Leu22641=
ENST00000589042.5:c.95116C= (TTN) MANE Select ENSP00000467141.1:p.Leu31706=
ENST00000591111.5:c.90193C= (TTN) ENSP00000465570.1:p.Leu30065=
ENST00000615779.4:c.90193C= (TTN) ENSP00000483597.1:p.Leu30065=
NM_001256850.1:c.90193C= (TTN) NP_001243779.1:p.Leu30065=
NM_001267550.2:c.95116C= (TTN) MANE Select NP_001254479.2:p.Leu31706=
NM_003319.4:c.67921C= (TTN) NP_003310.4:p.Leu22641=
NM_133378.4:c.87412C= (TTN) NP_596869.4:p.Leu29138=
NM_133432.3:c.68296C= (TTN) NP_597676.3:p.Leu22766=
NM_133437.4:c.68497C= (TTN) NP_597681.4:p.Leu22833=
NR_038271.1:n.446+22579G= (TTN-AS1)
NR_038272.1:n.2043+3854G= (TTN-AS1)
XM_011511729.1:c.94213C= (TTN) XP_011510031.1:p.Leu31405=
XM_011511730.1:c.68107C= (TTN) XP_011510032.1:p.Leu22703=
XM_011511731.1:c.67966C= (TTN) XP_011510033.1:p.Leu22656=
XM_017004819.1:c.94009C= (TTN) XP_016860308.1:p.Leu31337=
XM_017004820.1:c.89407C= (TTN) XP_016860309.1:p.Leu29803=
XM_017004821.1:c.89404C= (TTN) XP_016860310.1:p.Leu29802=
XM_017004822.1:c.86446C= (TTN) XP_016860311.1:p.Leu28816=
XM_017004823.1:c.68062C= (TTN) XP_016860312.1:p.Leu22688=
XM_024453094.1:c.89557C= (TTN) XP_024308862.1:p.Leu29853=
XM_024453095.1:c.89554C= (TTN) XP_024308863.1:p.Leu29852=
XM_024453096.1:c.88987C= (TTN) XP_024308864.1:p.Leu29663=
XM_024453097.1:c.86329C= (TTN) XP_024308865.1:p.Leu28777=
XM_024453098.1:c.86248C= (TTN) XP_024308866.1:p.Leu28750=
XM_024453099.1:c.68011C= (TTN) XP_024308867.1:p.Leu22671=
XM_024453100.1:c.57865C= (TTN) XP_024308868.1:p.Leu19289=