Canonical Allele Identifier: CA1310550890

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178618054G= , CM000664.2:g.178618054G= GRCh38
NC_000002.11:g.179482781G= , CM000664.1:g.179482781G= GRCh37
NC_000002.10:g.179191026G= NCBI36
NG_011618.3:g.217749C= , LRG_391:g.217749C=
NG_051363.1:g.100228G=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.39593C= (TTN) ENSP00000343764.6:p.Thr13198=
ENST00000342175.11:c.20678C= (TTN) ENSP00000340554.6:p.Thr6893=
ENST00000359218.10:c.20477C= (TTN) ENSP00000352154.5:p.Thr6826=
ENST00000342175.10:c.20678C= (TTN) ENSP00000340554.6:p.Thr6893=
ENST00000342992.10:c.39593C= (TTN) ENSP00000343764.6:p.Thr13198=
ENST00000359218.9:c.20477C= (TTN) ENSP00000352154.5:p.Thr6826=
ENST00000460472.6:c.20102C= (TTN) ENSP00000434586.1:p.Thr6701=
ENST00000589042.5:c.47297C= (TTN) MANE Select ENSP00000467141.1:p.Thr15766=
ENST00000591111.5:c.42374C= (TTN) ENSP00000465570.1:p.Thr14125=
ENST00000615779.4:c.42374C= (TTN) ENSP00000483597.1:p.Thr14125=
NM_001256850.1:c.42374C= (TTN) NP_001243779.1:p.Thr14125=
NM_001267550.2:c.47297C= (TTN) MANE Select NP_001254479.2:p.Thr15766=
NM_003319.4:c.20102C= (TTN) NP_003310.4:p.Thr6701=
NM_133378.4:c.39593C= (TTN) NP_596869.4:p.Thr13198=
NM_133432.3:c.20477C= (TTN) NP_597676.3:p.Thr6826=
NM_133437.4:c.20678C= (TTN) NP_597681.4:p.Thr6893=
NR_038271.1:n.1605-1699G= (TTN-AS1)
XM_011511729.1:c.46394C= (TTN) XP_011510031.1:p.Thr15465=
XM_011511730.1:c.20288C= (TTN) XP_011510032.1:p.Thr6763=
XM_011511731.1:c.20147C= (TTN) XP_011510033.1:p.Thr6716=
XM_017004819.1:c.46190C= (TTN) XP_016860308.1:p.Thr15397=
XM_017004820.1:c.41588C= (TTN) XP_016860309.1:p.Thr13863=
XM_017004821.1:c.41585C= (TTN) XP_016860310.1:p.Thr13862=
XM_017004822.1:c.38627C= (TTN) XP_016860311.1:p.Thr12876=
XM_017004823.1:c.20243C= (TTN) XP_016860312.1:p.Thr6748=
XM_024453094.1:c.41738C= (TTN) XP_024308862.1:p.Thr13913=
XM_024453095.1:c.41735C= (TTN) XP_024308863.1:p.Thr13912=
XM_024453096.1:c.41168C= (TTN) XP_024308864.1:p.Thr13723=
XM_024453097.1:c.38510C= (TTN) XP_024308865.1:p.Thr12837=
XM_024453098.1:c.38429C= (TTN) XP_024308866.1:p.Thr12810=
XM_024453099.1:c.20192C= (TTN) XP_024308867.1:p.Thr6731=
XM_024453100.1:c.10046C= (TTN) XP_024308868.1:p.Thr3349=