Canonical Allele Identifier: CA1310515282

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178537173C= , CM000664.2:g.178537173C= GRCh38
NC_000002.11:g.179401900C= , CM000664.1:g.179401900C= GRCh37
NC_000002.10:g.179110146C= NCBI36
NG_011618.3:g.298630G= , LRG_391:g.298630G=
NG_051363.1:g.19347C=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.92232G= (TTN) ENSP00000343764.6:p.Trp30744=
ENST00000342175.11:c.73317G= (TTN) ENSP00000340554.6:p.Trp24439=
ENST00000359218.10:c.73116G= (TTN) ENSP00000352154.5:p.Trp24372=
ENST00000342175.10:c.73317G= (TTN) ENSP00000340554.6:p.Trp24439=
ENST00000342992.10:c.92232G= (TTN) ENSP00000343764.6:p.Trp30744=
ENST00000359218.9:c.73116G= (TTN) ENSP00000352154.5:p.Trp24372=
ENST00000460472.6:c.72741G= (TTN) ENSP00000434586.1:p.Trp24247=
ENST00000589042.5:c.99936G= (TTN) MANE Select ENSP00000467141.1:p.Trp33312=
ENST00000591111.5:c.95013G= (TTN) ENSP00000465570.1:p.Trp31671=
ENST00000615779.4:c.95013G= (TTN) ENSP00000483597.1:p.Trp31671=
NM_001256850.1:c.95013G= (TTN) NP_001243779.1:p.Trp31671=
NM_001267550.2:c.99936G= (TTN) MANE Select NP_001254479.2:p.Trp33312=
NM_003319.4:c.72741G= (TTN) NP_003310.4:p.Trp24247=
NM_133378.4:c.92232G= (TTN) NP_596869.4:p.Trp30744=
NM_133432.3:c.73116G= (TTN) NP_597676.3:p.Trp24372=
NM_133437.4:c.73317G= (TTN) NP_597681.4:p.Trp24439=
NR_038271.1:n.446+13537C= (TTN-AS1)
NR_038272.1:n.317-188C= (TTN-AS1)
XM_011511729.1:c.99033G= (TTN) XP_011510031.1:p.Trp33011=
XM_011511730.1:c.72927G= (TTN) XP_011510032.1:p.Trp24309=
XM_011511731.1:c.72786G= (TTN) XP_011510033.1:p.Trp24262=
XM_017004819.1:c.98829G= (TTN) XP_016860308.1:p.Trp32943=
XM_017004820.1:c.94227G= (TTN) XP_016860309.1:p.Trp31409=
XM_017004821.1:c.94224G= (TTN) XP_016860310.1:p.Trp31408=
XM_017004822.1:c.91266G= (TTN) XP_016860311.1:p.Trp30422=
XM_017004823.1:c.72882G= (TTN) XP_016860312.1:p.Trp24294=
XM_024453094.1:c.94377G= (TTN) XP_024308862.1:p.Trp31459=
XM_024453095.1:c.94374G= (TTN) XP_024308863.1:p.Trp31458=
XM_024453096.1:c.93807G= (TTN) XP_024308864.1:p.Trp31269=
XM_024453097.1:c.91149G= (TTN) XP_024308865.1:p.Trp30383=
XM_024453098.1:c.91068G= (TTN) XP_024308866.1:p.Trp30356=
XM_024453099.1:c.72831G= (TTN) XP_024308867.1:p.Trp24277=
XM_024453100.1:c.62685G= (TTN) XP_024308868.1:p.Trp20895=