Canonical Allele Identifier: CA1310520128

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178549836A= , CM000664.2:g.178549836A= GRCh38
NC_000002.11:g.179414563A= , CM000664.1:g.179414563A= GRCh37
NC_000002.10:g.179122809A= NCBI36
NG_011618.3:g.285967T= , LRG_391:g.285967T=
NG_051363.1:g.32010A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.84182T= (TTN) ENSP00000343764.6:p.Phe28061=
ENST00000342175.11:c.65267T= (TTN) ENSP00000340554.6:p.Phe21756=
ENST00000359218.10:c.65066T= (TTN) ENSP00000352154.5:p.Phe21689=
ENST00000342175.10:c.65267T= (TTN) ENSP00000340554.6:p.Phe21756=
ENST00000342992.10:c.84182T= (TTN) ENSP00000343764.6:p.Phe28061=
ENST00000359218.9:c.65066T= (TTN) ENSP00000352154.5:p.Phe21689=
ENST00000460472.6:c.64691T= (TTN) ENSP00000434586.1:p.Phe21564=
ENST00000589042.5:c.91886T= (TTN) MANE Select ENSP00000467141.1:p.Phe30629=
ENST00000591111.5:c.86963T= (TTN) ENSP00000465570.1:p.Phe28988=
ENST00000615779.4:c.86963T= (TTN) ENSP00000483597.1:p.Phe28988=
NM_001256850.1:c.86963T= (TTN) NP_001243779.1:p.Phe28988=
NM_001267550.2:c.91886T= (TTN) MANE Select NP_001254479.2:p.Phe30629=
NM_003319.4:c.64691T= (TTN) NP_003310.4:p.Phe21564=
NM_133378.4:c.84182T= (TTN) NP_596869.4:p.Phe28061=
NM_133432.3:c.65066T= (TTN) NP_597676.3:p.Phe21689=
NM_133437.4:c.65267T= (TTN) NP_597681.4:p.Phe21756=
NR_038271.1:n.447-21464A= (TTN-AS1)
NR_038272.1:n.2043+7475A= (TTN-AS1)
XM_011511729.1:c.90983T= (TTN) XP_011510031.1:p.Phe30328=
XM_011511730.1:c.64877T= (TTN) XP_011510032.1:p.Phe21626=
XM_011511731.1:c.64736T= (TTN) XP_011510033.1:p.Phe21579=
XM_017004819.1:c.90779T= (TTN) XP_016860308.1:p.Phe30260=
XM_017004820.1:c.86177T= (TTN) XP_016860309.1:p.Phe28726=
XM_017004821.1:c.86174T= (TTN) XP_016860310.1:p.Phe28725=
XM_017004822.1:c.83216T= (TTN) XP_016860311.1:p.Phe27739=
XM_017004823.1:c.64832T= (TTN) XP_016860312.1:p.Phe21611=
XM_024453094.1:c.86327T= (TTN) XP_024308862.1:p.Phe28776=
XM_024453095.1:c.86324T= (TTN) XP_024308863.1:p.Phe28775=
XM_024453096.1:c.85757T= (TTN) XP_024308864.1:p.Phe28586=
XM_024453097.1:c.83099T= (TTN) XP_024308865.1:p.Phe27700=
XM_024453098.1:c.83018T= (TTN) XP_024308866.1:p.Phe27673=
XM_024453099.1:c.64781T= (TTN) XP_024308867.1:p.Phe21594=
XM_024453100.1:c.54635T= (TTN) XP_024308868.1:p.Phe18212=