Canonical Allele Identifier: CA1310523476

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178546867A= , CM000664.2:g.178546867A= GRCh38
NC_000002.11:g.179411594A= , CM000664.1:g.179411594A= GRCh37
NC_000002.10:g.179119840A= NCBI36
NG_011618.3:g.288936T= , LRG_391:g.288936T=
NG_051363.1:g.29041A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.86857T= (TTN) ENSP00000343764.6:p.Ser28953=
ENST00000342175.11:c.67942T= (TTN) ENSP00000340554.6:p.Ser22648=
ENST00000359218.10:c.67741T= (TTN) ENSP00000352154.5:p.Ser22581=
ENST00000342175.10:c.67942T= (TTN) ENSP00000340554.6:p.Ser22648=
ENST00000342992.10:c.86857T= (TTN) ENSP00000343764.6:p.Ser28953=
ENST00000359218.9:c.67741T= (TTN) ENSP00000352154.5:p.Ser22581=
ENST00000460472.6:c.67366T= (TTN) ENSP00000434586.1:p.Ser22456=
ENST00000589042.5:c.94561T= (TTN) MANE Select ENSP00000467141.1:p.Ser31521=
ENST00000591111.5:c.89638T= (TTN) ENSP00000465570.1:p.Ser29880=
ENST00000615779.4:c.89638T= (TTN) ENSP00000483597.1:p.Ser29880=
NM_001256850.1:c.89638T= (TTN) NP_001243779.1:p.Ser29880=
NM_001267550.2:c.94561T= (TTN) MANE Select NP_001254479.2:p.Ser31521=
NM_003319.4:c.67366T= (TTN) NP_003310.4:p.Ser22456=
NM_133378.4:c.86857T= (TTN) NP_596869.4:p.Ser28953=
NM_133432.3:c.67741T= (TTN) NP_597676.3:p.Ser22581=
NM_133437.4:c.67942T= (TTN) NP_597681.4:p.Ser22648=
NR_038271.1:n.446+23231A= (TTN-AS1)
NR_038272.1:n.2043+4506A= (TTN-AS1)
XM_011511729.1:c.93658T= (TTN) XP_011510031.1:p.Ser31220=
XM_011511730.1:c.67552T= (TTN) XP_011510032.1:p.Ser22518=
XM_011511731.1:c.67411T= (TTN) XP_011510033.1:p.Ser22471=
XM_017004819.1:c.93454T= (TTN) XP_016860308.1:p.Ser31152=
XM_017004820.1:c.88852T= (TTN) XP_016860309.1:p.Ser29618=
XM_017004821.1:c.88849T= (TTN) XP_016860310.1:p.Ser29617=
XM_017004822.1:c.85891T= (TTN) XP_016860311.1:p.Ser28631=
XM_017004823.1:c.67507T= (TTN) XP_016860312.1:p.Ser22503=
XM_024453094.1:c.89002T= (TTN) XP_024308862.1:p.Ser29668=
XM_024453095.1:c.88999T= (TTN) XP_024308863.1:p.Ser29667=
XM_024453096.1:c.88432T= (TTN) XP_024308864.1:p.Ser29478=
XM_024453097.1:c.85774T= (TTN) XP_024308865.1:p.Ser28592=
XM_024453098.1:c.85693T= (TTN) XP_024308866.1:p.Ser28565=
XM_024453099.1:c.67456T= (TTN) XP_024308867.1:p.Ser22486=
XM_024453100.1:c.57310T= (TTN) XP_024308868.1:p.Ser19104=