Canonical Allele Identifier: CA1310532381

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178574037T= , CM000664.2:g.178574037T= GRCh38
NC_000002.11:g.179438764T= , CM000664.1:g.179438764T= GRCh37
NC_000002.10:g.179147010T= NCBI36
NG_011618.3:g.261766A= , LRG_391:g.261766A=
NG_051363.1:g.56211T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.64391A= (TTN) ENSP00000343764.6:p.Asp21464=
ENST00000342175.11:c.45476A= (TTN) ENSP00000340554.6:p.Asp15159=
ENST00000359218.10:c.45275A= (TTN) ENSP00000352154.5:p.Asp15092=
ENST00000342175.10:c.45476A= (TTN) ENSP00000340554.6:p.Asp15159=
ENST00000342992.10:c.64391A= (TTN) ENSP00000343764.6:p.Asp21464=
ENST00000359218.9:c.45275A= (TTN) ENSP00000352154.5:p.Asp15092=
ENST00000460472.6:c.44900A= (TTN) ENSP00000434586.1:p.Asp14967=
ENST00000589042.5:c.72095A= (TTN) MANE Select ENSP00000467141.1:p.Asp24032=
ENST00000591111.5:c.67172A= (TTN) ENSP00000465570.1:p.Asp22391=
ENST00000615779.4:c.67172A= (TTN) ENSP00000483597.1:p.Asp22391=
NM_001256850.1:c.67172A= (TTN) NP_001243779.1:p.Asp22391=
NM_001267550.2:c.72095A= (TTN) MANE Select NP_001254479.2:p.Asp24032=
NM_003319.4:c.44900A= (TTN) NP_003310.4:p.Asp14967=
NM_133378.4:c.64391A= (TTN) NP_596869.4:p.Asp21464=
NM_133432.3:c.45275A= (TTN) NP_597676.3:p.Asp15092=
NM_133437.4:c.45476A= (TTN) NP_597681.4:p.Asp15159=
NR_038271.1:n.596+2588T= (TTN-AS1)
NR_038272.1:n.2044-8535T= (TTN-AS1)
XM_011511729.1:c.71192A= (TTN) XP_011510031.1:p.Asp23731=
XM_011511730.1:c.45086A= (TTN) XP_011510032.1:p.Asp15029=
XM_011511731.1:c.44945A= (TTN) XP_011510033.1:p.Asp14982=
XM_017004819.1:c.70988A= (TTN) XP_016860308.1:p.Asp23663=
XM_017004820.1:c.66386A= (TTN) XP_016860309.1:p.Asp22129=
XM_017004821.1:c.66383A= (TTN) XP_016860310.1:p.Asp22128=
XM_017004822.1:c.63425A= (TTN) XP_016860311.1:p.Asp21142=
XM_017004823.1:c.45041A= (TTN) XP_016860312.1:p.Asp15014=
XM_024453094.1:c.66536A= (TTN) XP_024308862.1:p.Asp22179=
XM_024453095.1:c.66533A= (TTN) XP_024308863.1:p.Asp22178=
XM_024453096.1:c.65966A= (TTN) XP_024308864.1:p.Asp21989=
XM_024453097.1:c.63308A= (TTN) XP_024308865.1:p.Asp21103=
XM_024453098.1:c.63227A= (TTN) XP_024308866.1:p.Asp21076=
XM_024453099.1:c.44990A= (TTN) XP_024308867.1:p.Asp14997=
XM_024453100.1:c.34844A= (TTN) XP_024308868.1:p.Asp11615=