Canonical Allele Identifier: CA1310553530
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178624506T= , CM000664.2:g.178624506T= GRCh38
NC_000002.11:g.179489233T= , CM000664.1:g.179489233T= GRCh37
NC_000002.10:g.179197478T= NCBI36
NG_011618.3:g.211297A= , LRG_391:g.211297A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.37070A= ENSP00000343764.6:p.Asp12357=
ENST00000342175.11:c.18155A= ENSP00000340554.6:p.Asp6052=
ENST00000359218.10:c.17954A= ENSP00000352154.5:p.Asp5985=
ENST00000342175.10:c.18155A= ENSP00000340554.6:p.Asp6052=
ENST00000342992.10:c.37070A= ENSP00000343764.6:p.Asp12357=
ENST00000359218.9:c.17954A= ENSP00000352154.5:p.Asp5985=
ENST00000460472.6:c.17579A= ENSP00000434586.1:p.Asp5860=
ENST00000589042.5:c.44774A= MANE Select ENSP00000467141.1:p.Asp14925=
ENST00000591111.5:c.39851A= ENSP00000465570.1:p.Asp13284=
ENST00000615779.4:c.39851A= ENSP00000483597.1:p.Asp13284=
NM_001256850.1:c.39851A= NP_001243779.1:p.Asp13284=
NM_001267550.2:c.44774A= MANE Select NP_001254479.2:p.Asp14925=
NM_003319.4:c.17579A= NP_003310.4:p.Asp5860=
NM_133378.4:c.37070A= NP_596869.4:p.Asp12357=
NM_133432.3:c.17954A= NP_597676.3:p.Asp5985=
NM_133437.4:c.18155A= NP_597681.4:p.Asp6052=
XM_011511729.1:c.43871A= XP_011510031.1:p.Asp14624=
XM_011511730.1:c.17765A= XP_011510032.1:p.Asp5922=
XM_011511731.1:c.17624A= XP_011510033.1:p.Asp5875=
XM_017004819.1:c.43667A= XP_016860308.1:p.Asp14556=
XM_017004820.1:c.39065A= XP_016860309.1:p.Asp13022=
XM_017004821.1:c.39062A= XP_016860310.1:p.Asp13021=
XM_017004822.1:c.36104A= XP_016860311.1:p.Asp12035=
XM_017004823.1:c.17720A= XP_016860312.1:p.Asp5907=
XM_024453094.1:c.39215A= XP_024308862.1:p.Asp13072=
XM_024453095.1:c.39212A= XP_024308863.1:p.Asp13071=
XM_024453096.1:c.38645A= XP_024308864.1:p.Asp12882=
XM_024453097.1:c.35987A= XP_024308865.1:p.Asp11996=
XM_024453098.1:c.35906A= XP_024308866.1:p.Asp11969=
XM_024453099.1:c.17669A= XP_024308867.1:p.Asp5890=
XM_024453100.1:c.7523A= XP_024308868.1:p.Asp2508=