Canonical Allele Identifier: CA1310601312
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178740382T= , CM000664.2:g.178740382T= GRCh38
NC_000002.11:g.179605109T= , CM000664.1:g.179605109T= GRCh37
NC_000002.10:g.179313354T= NCBI36
NG_011618.3:g.95421A= , LRG_391:g.95421A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.10361-2022A= ENSP00000343764.6:n.10361-2022A=
ENST00000342175.11:c.12338A= ENSP00000340554.6:p.Gln4113=
ENST00000359218.10:c.12137A= ENSP00000352154.5:p.Gln4046=
ENST00000342175.10:c.12338A= ENSP00000340554.6:p.Gln4113=
ENST00000342992.10:c.10361-2022A= ENSP00000343764.6:n.10361-2022A=
ENST00000359218.9:c.12137A= ENSP00000352154.5:p.Gln4046=
ENST00000460472.6:c.11762A= ENSP00000434586.1:p.Gln3921=
ENST00000589042.5:c.12851A= MANE Select ENSP00000467141.1:p.Gln4284=
ENST00000591111.5:c.11900A= ENSP00000465570.1:p.Gln3967=
ENST00000615779.4:c.11900A= ENSP00000483597.1:p.Gln3967=
NM_001256850.1:c.11900A= NP_001243779.1:p.Gln3967=
NM_001267550.2:c.12851A= MANE Select NP_001254479.2:p.Gln4284=
NM_003319.4:c.11762A= NP_003310.4:p.Gln3921=
NM_133378.4:c.10361-2022A= NP_596869.4:n.10361-2022A=
NM_133432.3:c.12137A= NP_597676.3:p.Gln4046=
NM_133437.4:c.12338A= NP_597681.4:p.Gln4113=
XM_011511729.1:c.11948A= XP_011510031.1:p.Gln3983=
XM_011511730.1:c.11948A= XP_011510032.1:p.Gln3983=
XM_011511731.1:c.11807A= XP_011510033.1:p.Gln3936=
XM_017004819.1:c.11903A= XP_016860308.1:p.Gln3968=
XM_017004820.1:c.10364-2022A= XP_016860309.1:n.10364-2022A=
XM_017004821.1:c.10361-2022A= XP_016860310.1:n.10361-2022A=
XM_017004822.1:c.11903A= XP_016860311.1:p.Gln3968=
XM_017004823.1:c.11903A= XP_016860312.1:p.Gln3968=
XM_024453094.1:c.11903A= XP_024308862.1:p.Gln3968=
XM_024453095.1:c.11903A= XP_024308863.1:p.Gln3968=
XM_024453096.1:c.11903A= XP_024308864.1:p.Gln3968=
XM_024453097.1:c.11903A= XP_024308865.1:p.Gln3968=
XM_024453098.1:c.11903A= XP_024308866.1:p.Gln3968=
XM_024453099.1:c.11903A= XP_024308867.1:p.Gln3968=