Canonical Allele Identifier: CA1310550938

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178618157A= , CM000664.2:g.178618157A= GRCh38
NC_000002.11:g.179482884A= , CM000664.1:g.179482884A= GRCh37
NC_000002.10:g.179191129A= NCBI36
NG_011618.3:g.217646T= , LRG_391:g.217646T=
NG_051363.1:g.100331A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.39565+32T= (TTN) ENSP00000343764.6:n.39565+32T=
ENST00000342175.11:c.20650+32T= (TTN) ENSP00000340554.6:n.20650+32T=
ENST00000359218.10:c.20449+32T= (TTN) ENSP00000352154.5:n.20449+32T=
ENST00000342175.10:c.20650+32T= (TTN) ENSP00000340554.6:n.20650+32T=
ENST00000342992.10:c.39565+32T= (TTN) ENSP00000343764.6:n.39565+32T=
ENST00000359218.9:c.20449+32T= (TTN) ENSP00000352154.5:n.20449+32T=
ENST00000460472.6:c.20074+32T= (TTN) ENSP00000434586.1:n.20074+32T=
ENST00000589042.5:c.47269+32T= (TTN) MANE Select ENSP00000467141.1:n.47269+32T=
ENST00000591111.5:c.42346+32T= (TTN) ENSP00000465570.1:n.42346+32T=
ENST00000615779.4:c.42346+32T= (TTN) ENSP00000483597.1:n.42346+32T=
NM_001256850.1:c.42346+32T= (TTN) NP_001243779.1:n.42346+32T=
NM_001267550.2:c.47269+32T= (TTN) MANE Select NP_001254479.2:n.47269+32T=
NM_003319.4:c.20074+32T= (TTN) NP_003310.4:n.20074+32T=
NM_133378.4:c.39565+32T= (TTN) NP_596869.4:n.39565+32T=
NM_133432.3:c.20449+32T= (TTN) NP_597676.3:n.20449+32T=
NM_133437.4:c.20650+32T= (TTN) NP_597681.4:n.20650+32T=
NR_038271.1:n.1605-1596A= (TTN-AS1)
XM_011511729.1:c.46366+32T= (TTN) XP_011510031.1:n.46366+32T=
XM_011511730.1:c.20260+32T= (TTN) XP_011510032.1:n.20260+32T=
XM_011511731.1:c.20119+32T= (TTN) XP_011510033.1:n.20119+32T=
XM_017004819.1:c.46162+32T= (TTN) XP_016860308.1:n.46162+32T=
XM_017004820.1:c.41560+32T= (TTN) XP_016860309.1:n.41560+32T=
XM_017004821.1:c.41557+32T= (TTN) XP_016860310.1:n.41557+32T=
XM_017004822.1:c.38599+32T= (TTN) XP_016860311.1:n.38599+32T=
XM_017004823.1:c.20215+32T= (TTN) XP_016860312.1:n.20215+32T=
XM_024453094.1:c.41710+32T= (TTN) XP_024308862.1:n.41710+32T=
XM_024453095.1:c.41707+32T= (TTN) XP_024308863.1:n.41707+32T=
XM_024453096.1:c.41140+32T= (TTN) XP_024308864.1:n.41140+32T=
XM_024453097.1:c.38482+32T= (TTN) XP_024308865.1:n.38482+32T=
XM_024453098.1:c.38401+32T= (TTN) XP_024308866.1:n.38401+32T=
XM_024453099.1:c.20164+32T= (TTN) XP_024308867.1:n.20164+32T=
XM_024453100.1:c.10018+32T= (TTN) XP_024308868.1:n.10018+32T=