Canonical Allele Identifier: CA1310518151

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178532266G= , CM000664.2:g.178532266G= GRCh38
NC_000002.11:g.179396993G= , CM000664.1:g.179396993G= GRCh37
NC_000002.10:g.179105239G= NCBI36
NG_011618.3:g.303537C= , LRG_391:g.303537C=
NG_051363.1:g.14440G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.96645C= (TTN) ENSP00000343764.6:p.Leu32215=
ENST00000342175.11:c.77730C= (TTN) ENSP00000340554.6:p.Leu25910=
ENST00000359218.10:c.77529C= (TTN) ENSP00000352154.5:p.Leu25843=
ENST00000342175.10:c.77730C= (TTN) ENSP00000340554.6:p.Leu25910=
ENST00000342992.10:c.96645C= (TTN) ENSP00000343764.6:p.Leu32215=
ENST00000359218.9:c.77529C= (TTN) ENSP00000352154.5:p.Leu25843=
ENST00000460472.6:c.77154C= (TTN) ENSP00000434586.1:p.Leu25718=
ENST00000589042.5:c.104349C= (TTN) MANE Select ENSP00000467141.1:p.Leu34783=
ENST00000591111.5:c.99426C= (TTN) ENSP00000465570.1:p.Leu33142=
ENST00000615779.4:c.99426C= (TTN) ENSP00000483597.1:p.Leu33142=
NM_001256850.1:c.99426C= (TTN) NP_001243779.1:p.Leu33142=
NM_001267550.2:c.104349C= (TTN) MANE Select NP_001254479.2:p.Leu34783=
NM_003319.4:c.77154C= (TTN) NP_003310.4:p.Leu25718=
NM_133378.4:c.96645C= (TTN) NP_596869.4:p.Leu32215=
NM_133432.3:c.77529C= (TTN) NP_597676.3:p.Leu25843=
NM_133437.4:c.77730C= (TTN) NP_597681.4:p.Leu25910=
NR_038271.1:n.446+8630G= (TTN-AS1)
NR_038272.1:n.220-3466G= (TTN-AS1)
XM_011511729.1:c.103446C= (TTN) XP_011510031.1:p.Leu34482=
XM_011511730.1:c.77340C= (TTN) XP_011510032.1:p.Leu25780=
XM_011511731.1:c.77199C= (TTN) XP_011510033.1:p.Leu25733=
XM_017004819.1:c.103242C= (TTN) XP_016860308.1:p.Leu34414=
XM_017004820.1:c.98640C= (TTN) XP_016860309.1:p.Leu32880=
XM_017004821.1:c.98637C= (TTN) XP_016860310.1:p.Leu32879=
XM_017004822.1:c.95679C= (TTN) XP_016860311.1:p.Leu31893=
XM_017004823.1:c.77295C= (TTN) XP_016860312.1:p.Leu25765=
XM_024453094.1:c.98790C= (TTN) XP_024308862.1:p.Leu32930=
XM_024453095.1:c.98787C= (TTN) XP_024308863.1:p.Leu32929=
XM_024453096.1:c.98220C= (TTN) XP_024308864.1:p.Leu32740=
XM_024453097.1:c.95562C= (TTN) XP_024308865.1:p.Leu31854=
XM_024453098.1:c.95481C= (TTN) XP_024308866.1:p.Leu31827=
XM_024453099.1:c.77244C= (TTN) XP_024308867.1:p.Leu25748=
XM_024453100.1:c.67098C= (TTN) XP_024308868.1:p.Leu22366=