Canonical Allele Identifier: CA1310601415
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178740492C= , CM000664.2:g.178740492C= GRCh38
NC_000002.11:g.179605219C= , CM000664.1:g.179605219C= GRCh37
NC_000002.10:g.179313464C= NCBI36
NG_011618.3:g.95311G= , LRG_391:g.95311G=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.10361-2132G= ENSP00000343764.6:n.10361-2132G=
ENST00000342175.11:c.12228G= ENSP00000340554.6:p.Glu4076=
ENST00000359218.10:c.12027G= ENSP00000352154.5:p.Glu4009=
ENST00000342175.10:c.12228G= ENSP00000340554.6:p.Glu4076=
ENST00000342992.10:c.10361-2132G= ENSP00000343764.6:n.10361-2132G=
ENST00000359218.9:c.12027G= ENSP00000352154.5:p.Glu4009=
ENST00000460472.6:c.11652G= ENSP00000434586.1:p.Glu3884=
ENST00000589042.5:c.12741G= MANE Select ENSP00000467141.1:p.Glu4247=
ENST00000591111.5:c.11790G= ENSP00000465570.1:p.Glu3930=
ENST00000615779.4:c.11790G= ENSP00000483597.1:p.Glu3930=
NM_001256850.1:c.11790G= NP_001243779.1:p.Glu3930=
NM_001267550.2:c.12741G= MANE Select NP_001254479.2:p.Glu4247=
NM_003319.4:c.11652G= NP_003310.4:p.Glu3884=
NM_133378.4:c.10361-2132G= NP_596869.4:n.10361-2132G=
NM_133432.3:c.12027G= NP_597676.3:p.Glu4009=
NM_133437.4:c.12228G= NP_597681.4:p.Glu4076=
XM_011511729.1:c.11838G= XP_011510031.1:p.Glu3946=
XM_011511730.1:c.11838G= XP_011510032.1:p.Glu3946=
XM_011511731.1:c.11697G= XP_011510033.1:p.Glu3899=
XM_017004819.1:c.11793G= XP_016860308.1:p.Glu3931=
XM_017004820.1:c.10364-2132G= XP_016860309.1:n.10364-2132G=
XM_017004821.1:c.10361-2132G= XP_016860310.1:n.10361-2132G=
XM_017004822.1:c.11793G= XP_016860311.1:p.Glu3931=
XM_017004823.1:c.11793G= XP_016860312.1:p.Glu3931=
XM_024453094.1:c.11793G= XP_024308862.1:p.Glu3931=
XM_024453095.1:c.11793G= XP_024308863.1:p.Glu3931=
XM_024453096.1:c.11793G= XP_024308864.1:p.Glu3931=
XM_024453097.1:c.11793G= XP_024308865.1:p.Glu3931=
XM_024453098.1:c.11793G= XP_024308866.1:p.Glu3931=
XM_024453099.1:c.11793G= XP_024308867.1:p.Glu3931=