Canonical Allele Identifier: CA1310550905

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178618080A= , CM000664.2:g.178618080A= GRCh38
NC_000002.11:g.179482807A= , CM000664.1:g.179482807A= GRCh37
NC_000002.10:g.179191052A= NCBI36
NG_011618.3:g.217723T= , LRG_391:g.217723T=
NG_051363.1:g.100254A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.39567T= (TTN) ENSP00000343764.6:p.Asp13189=
ENST00000342175.11:c.20652T= (TTN) ENSP00000340554.6:p.Asp6884=
ENST00000359218.10:c.20451T= (TTN) ENSP00000352154.5:p.Asp6817=
ENST00000342175.10:c.20652T= (TTN) ENSP00000340554.6:p.Asp6884=
ENST00000342992.10:c.39567T= (TTN) ENSP00000343764.6:p.Asp13189=
ENST00000359218.9:c.20451T= (TTN) ENSP00000352154.5:p.Asp6817=
ENST00000460472.6:c.20076T= (TTN) ENSP00000434586.1:p.Asp6692=
ENST00000589042.5:c.47271T= (TTN) MANE Select ENSP00000467141.1:p.Asp15757=
ENST00000591111.5:c.42348T= (TTN) ENSP00000465570.1:p.Asp14116=
ENST00000615779.4:c.42348T= (TTN) ENSP00000483597.1:p.Asp14116=
NM_001256850.1:c.42348T= (TTN) NP_001243779.1:p.Asp14116=
NM_001267550.2:c.47271T= (TTN) MANE Select NP_001254479.2:p.Asp15757=
NM_003319.4:c.20076T= (TTN) NP_003310.4:p.Asp6692=
NM_133378.4:c.39567T= (TTN) NP_596869.4:p.Asp13189=
NM_133432.3:c.20451T= (TTN) NP_597676.3:p.Asp6817=
NM_133437.4:c.20652T= (TTN) NP_597681.4:p.Asp6884=
NR_038271.1:n.1605-1673A= (TTN-AS1)
XM_011511729.1:c.46368T= (TTN) XP_011510031.1:p.Asp15456=
XM_011511730.1:c.20262T= (TTN) XP_011510032.1:p.Asp6754=
XM_011511731.1:c.20121T= (TTN) XP_011510033.1:p.Asp6707=
XM_017004819.1:c.46164T= (TTN) XP_016860308.1:p.Asp15388=
XM_017004820.1:c.41562T= (TTN) XP_016860309.1:p.Asp13854=
XM_017004821.1:c.41559T= (TTN) XP_016860310.1:p.Asp13853=
XM_017004822.1:c.38601T= (TTN) XP_016860311.1:p.Asp12867=
XM_017004823.1:c.20217T= (TTN) XP_016860312.1:p.Asp6739=
XM_024453094.1:c.41712T= (TTN) XP_024308862.1:p.Asp13904=
XM_024453095.1:c.41709T= (TTN) XP_024308863.1:p.Asp13903=
XM_024453096.1:c.41142T= (TTN) XP_024308864.1:p.Asp13714=
XM_024453097.1:c.38484T= (TTN) XP_024308865.1:p.Asp12828=
XM_024453098.1:c.38403T= (TTN) XP_024308866.1:p.Asp12801=
XM_024453099.1:c.20166T= (TTN) XP_024308867.1:p.Asp6722=
XM_024453100.1:c.10020T= (TTN) XP_024308868.1:p.Asp3340=