Canonical Allele Identifier: CA1310515527

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178537573A= , CM000664.2:g.178537573A= GRCh38
NC_000002.11:g.179402300A= , CM000664.1:g.179402300A= GRCh37
NC_000002.10:g.179110546A= NCBI36
NG_011618.3:g.298230T= , LRG_391:g.298230T=
NG_051363.1:g.19747A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.91930T= (TTN) ENSP00000343764.6:p.Ser30644=
ENST00000342175.11:c.73015T= (TTN) ENSP00000340554.6:p.Ser24339=
ENST00000359218.10:c.72814T= (TTN) ENSP00000352154.5:p.Ser24272=
ENST00000342175.10:c.73015T= (TTN) ENSP00000340554.6:p.Ser24339=
ENST00000342992.10:c.91930T= (TTN) ENSP00000343764.6:p.Ser30644=
ENST00000359218.9:c.72814T= (TTN) ENSP00000352154.5:p.Ser24272=
ENST00000460472.6:c.72439T= (TTN) ENSP00000434586.1:p.Ser24147=
ENST00000589042.5:c.99634T= (TTN) MANE Select ENSP00000467141.1:p.Ser33212=
ENST00000591111.5:c.94711T= (TTN) ENSP00000465570.1:p.Ser31571=
ENST00000615779.4:c.94711T= (TTN) ENSP00000483597.1:p.Ser31571=
NM_001256850.1:c.94711T= (TTN) NP_001243779.1:p.Ser31571=
NM_001267550.2:c.99634T= (TTN) MANE Select NP_001254479.2:p.Ser33212=
NM_003319.4:c.72439T= (TTN) NP_003310.4:p.Ser24147=
NM_133378.4:c.91930T= (TTN) NP_596869.4:p.Ser30644=
NM_133432.3:c.72814T= (TTN) NP_597676.3:p.Ser24272=
NM_133437.4:c.73015T= (TTN) NP_597681.4:p.Ser24339=
NR_038271.1:n.446+13937A= (TTN-AS1)
NR_038272.1:n.529A= (TTN-AS1)
XM_011511729.1:c.98731T= (TTN) XP_011510031.1:p.Ser32911=
XM_011511730.1:c.72625T= (TTN) XP_011510032.1:p.Ser24209=
XM_011511731.1:c.72484T= (TTN) XP_011510033.1:p.Ser24162=
XM_017004819.1:c.98527T= (TTN) XP_016860308.1:p.Ser32843=
XM_017004820.1:c.93925T= (TTN) XP_016860309.1:p.Ser31309=
XM_017004821.1:c.93922T= (TTN) XP_016860310.1:p.Ser31308=
XM_017004822.1:c.90964T= (TTN) XP_016860311.1:p.Ser30322=
XM_017004823.1:c.72580T= (TTN) XP_016860312.1:p.Ser24194=
XM_024453094.1:c.94075T= (TTN) XP_024308862.1:p.Ser31359=
XM_024453095.1:c.94072T= (TTN) XP_024308863.1:p.Ser31358=
XM_024453096.1:c.93505T= (TTN) XP_024308864.1:p.Ser31169=
XM_024453097.1:c.90847T= (TTN) XP_024308865.1:p.Ser30283=
XM_024453098.1:c.90766T= (TTN) XP_024308866.1:p.Ser30256=
XM_024453099.1:c.72529T= (TTN) XP_024308867.1:p.Ser24177=
XM_024453100.1:c.62383T= (TTN) XP_024308868.1:p.Ser20795=