Canonical Allele Identifier: CA1310526803

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178559831C= , CM000664.2:g.178559831C= GRCh38
NC_000002.11:g.179424558C= , CM000664.1:g.179424558C= GRCh37
NC_000002.10:g.179132804C= NCBI36
NG_011618.3:g.275972G= , LRG_391:g.275972G=
NG_051363.1:g.42005C=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.78597G= (TTN) ENSP00000343764.6:p.Lys26199=
ENST00000342175.11:c.59682G= (TTN) ENSP00000340554.6:p.Lys19894=
ENST00000359218.10:c.59481G= (TTN) ENSP00000352154.5:p.Lys19827=
ENST00000342175.10:c.59682G= (TTN) ENSP00000340554.6:p.Lys19894=
ENST00000342992.10:c.78597G= (TTN) ENSP00000343764.6:p.Lys26199=
ENST00000359218.9:c.59481G= (TTN) ENSP00000352154.5:p.Lys19827=
ENST00000460472.6:c.59106G= (TTN) ENSP00000434586.1:p.Lys19702=
ENST00000589042.5:c.86301G= (TTN) MANE Select ENSP00000467141.1:p.Lys28767=
ENST00000591111.5:c.81378G= (TTN) ENSP00000465570.1:p.Lys27126=
ENST00000615779.4:c.81378G= (TTN) ENSP00000483597.1:p.Lys27126=
NM_001256850.1:c.81378G= (TTN) NP_001243779.1:p.Lys27126=
NM_001267550.2:c.86301G= (TTN) MANE Select NP_001254479.2:p.Lys28767=
NM_003319.4:c.59106G= (TTN) NP_003310.4:p.Lys19702=
NM_133378.4:c.78597G= (TTN) NP_596869.4:p.Lys26199=
NM_133432.3:c.59481G= (TTN) NP_597676.3:p.Lys19827=
NM_133437.4:c.59682G= (TTN) NP_597681.4:p.Lys19894=
NR_038271.1:n.447-11469C= (TTN-AS1)
NR_038272.1:n.2043+17470C= (TTN-AS1)
XM_011511729.1:c.85398G= (TTN) XP_011510031.1:p.Lys28466=
XM_011511730.1:c.59292G= (TTN) XP_011510032.1:p.Lys19764=
XM_011511731.1:c.59151G= (TTN) XP_011510033.1:p.Lys19717=
XM_017004819.1:c.85194G= (TTN) XP_016860308.1:p.Lys28398=
XM_017004820.1:c.80592G= (TTN) XP_016860309.1:p.Lys26864=
XM_017004821.1:c.80589G= (TTN) XP_016860310.1:p.Lys26863=
XM_017004822.1:c.77631G= (TTN) XP_016860311.1:p.Lys25877=
XM_017004823.1:c.59247G= (TTN) XP_016860312.1:p.Lys19749=
XM_024453094.1:c.80742G= (TTN) XP_024308862.1:p.Lys26914=
XM_024453095.1:c.80739G= (TTN) XP_024308863.1:p.Lys26913=
XM_024453096.1:c.80172G= (TTN) XP_024308864.1:p.Lys26724=
XM_024453097.1:c.77514G= (TTN) XP_024308865.1:p.Lys25838=
XM_024453098.1:c.77433G= (TTN) XP_024308866.1:p.Lys25811=
XM_024453099.1:c.59196G= (TTN) XP_024308867.1:p.Lys19732=
XM_024453100.1:c.49050G= (TTN) XP_024308868.1:p.Lys16350=