Canonical Allele Identifier: CA1310522197

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178552678T= , CM000664.2:g.178552678T= GRCh38
NC_000002.11:g.179417405T= , CM000664.1:g.179417405T= GRCh37
NC_000002.10:g.179125651T= NCBI36
NG_011618.3:g.283125A= , LRG_391:g.283125A=
NG_051363.1:g.34852T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.82518A= (TTN) ENSP00000343764.6:p.Glu27506=
ENST00000342175.11:c.63603A= (TTN) ENSP00000340554.6:p.Glu21201=
ENST00000359218.10:c.63402A= (TTN) ENSP00000352154.5:p.Glu21134=
ENST00000342175.10:c.63603A= (TTN) ENSP00000340554.6:p.Glu21201=
ENST00000342992.10:c.82518A= (TTN) ENSP00000343764.6:p.Glu27506=
ENST00000359218.9:c.63402A= (TTN) ENSP00000352154.5:p.Glu21134=
ENST00000460472.6:c.63027A= (TTN) ENSP00000434586.1:p.Glu21009=
ENST00000589042.5:c.90222A= (TTN) MANE Select ENSP00000467141.1:p.Glu30074=
ENST00000591111.5:c.85299A= (TTN) ENSP00000465570.1:p.Glu28433=
ENST00000615779.4:c.85299A= (TTN) ENSP00000483597.1:p.Glu28433=
NM_001256850.1:c.85299A= (TTN) NP_001243779.1:p.Glu28433=
NM_001267550.2:c.90222A= (TTN) MANE Select NP_001254479.2:p.Glu30074=
NM_003319.4:c.63027A= (TTN) NP_003310.4:p.Glu21009=
NM_133378.4:c.82518A= (TTN) NP_596869.4:p.Glu27506=
NM_133432.3:c.63402A= (TTN) NP_597676.3:p.Glu21134=
NM_133437.4:c.63603A= (TTN) NP_597681.4:p.Glu21201=
NR_038271.1:n.447-18622T= (TTN-AS1)
NR_038272.1:n.2043+10317T= (TTN-AS1)
XM_011511729.1:c.89319A= (TTN) XP_011510031.1:p.Glu29773=
XM_011511730.1:c.63213A= (TTN) XP_011510032.1:p.Glu21071=
XM_011511731.1:c.63072A= (TTN) XP_011510033.1:p.Glu21024=
XM_017004819.1:c.89115A= (TTN) XP_016860308.1:p.Glu29705=
XM_017004820.1:c.84513A= (TTN) XP_016860309.1:p.Glu28171=
XM_017004821.1:c.84510A= (TTN) XP_016860310.1:p.Glu28170=
XM_017004822.1:c.81552A= (TTN) XP_016860311.1:p.Glu27184=
XM_017004823.1:c.63168A= (TTN) XP_016860312.1:p.Glu21056=
XM_024453094.1:c.84663A= (TTN) XP_024308862.1:p.Glu28221=
XM_024453095.1:c.84660A= (TTN) XP_024308863.1:p.Glu28220=
XM_024453096.1:c.84093A= (TTN) XP_024308864.1:p.Glu28031=
XM_024453097.1:c.81435A= (TTN) XP_024308865.1:p.Glu27145=
XM_024453098.1:c.81354A= (TTN) XP_024308866.1:p.Glu27118=
XM_024453099.1:c.63117A= (TTN) XP_024308867.1:p.Glu21039=
XM_024453100.1:c.52971A= (TTN) XP_024308868.1:p.Glu17657=