Canonical Allele Identifier: CA1310518030

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178532020A= , CM000664.2:g.178532020A= GRCh38
NC_000002.11:g.179396747A= , CM000664.1:g.179396747A= GRCh37
NC_000002.10:g.179104993A= NCBI36
NG_011618.3:g.303783T= , LRG_391:g.303783T=
NG_051363.1:g.14194A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.96891T= (TTN) ENSP00000343764.6:p.Ala32297=
ENST00000342175.11:c.77976T= (TTN) ENSP00000340554.6:p.Ala25992=
ENST00000359218.10:c.77775T= (TTN) ENSP00000352154.5:p.Ala25925=
ENST00000342175.10:c.77976T= (TTN) ENSP00000340554.6:p.Ala25992=
ENST00000342992.10:c.96891T= (TTN) ENSP00000343764.6:p.Ala32297=
ENST00000359218.9:c.77775T= (TTN) ENSP00000352154.5:p.Ala25925=
ENST00000460472.6:c.77400T= (TTN) ENSP00000434586.1:p.Ala25800=
ENST00000589042.5:c.104595T= (TTN) MANE Select ENSP00000467141.1:p.Ala34865=
ENST00000591111.5:c.99672T= (TTN) ENSP00000465570.1:p.Ala33224=
ENST00000615779.4:c.99672T= (TTN) ENSP00000483597.1:p.Ala33224=
NM_001256850.1:c.99672T= (TTN) NP_001243779.1:p.Ala33224=
NM_001267550.2:c.104595T= (TTN) MANE Select NP_001254479.2:p.Ala34865=
NM_003319.4:c.77400T= (TTN) NP_003310.4:p.Ala25800=
NM_133378.4:c.96891T= (TTN) NP_596869.4:p.Ala32297=
NM_133432.3:c.77775T= (TTN) NP_597676.3:p.Ala25925=
NM_133437.4:c.77976T= (TTN) NP_597681.4:p.Ala25992=
NR_038271.1:n.446+8384A= (TTN-AS1)
NR_038272.1:n.220-3712A= (TTN-AS1)
XM_011511729.1:c.103692T= (TTN) XP_011510031.1:p.Ala34564=
XM_011511730.1:c.77586T= (TTN) XP_011510032.1:p.Ala25862=
XM_011511731.1:c.77445T= (TTN) XP_011510033.1:p.Ala25815=
XM_017004819.1:c.103488T= (TTN) XP_016860308.1:p.Ala34496=
XM_017004820.1:c.98886T= (TTN) XP_016860309.1:p.Ala32962=
XM_017004821.1:c.98883T= (TTN) XP_016860310.1:p.Ala32961=
XM_017004822.1:c.95925T= (TTN) XP_016860311.1:p.Ala31975=
XM_017004823.1:c.77541T= (TTN) XP_016860312.1:p.Ala25847=
XM_024453094.1:c.99036T= (TTN) XP_024308862.1:p.Ala33012=
XM_024453095.1:c.99033T= (TTN) XP_024308863.1:p.Ala33011=
XM_024453096.1:c.98466T= (TTN) XP_024308864.1:p.Ala32822=
XM_024453097.1:c.95808T= (TTN) XP_024308865.1:p.Ala31936=
XM_024453098.1:c.95727T= (TTN) XP_024308866.1:p.Ala31909=
XM_024453099.1:c.77490T= (TTN) XP_024308867.1:p.Ala25830=
XM_024453100.1:c.67344T= (TTN) XP_024308868.1:p.Ala22448=