Canonical Allele Identifier: CA1310514285

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178527073C= , CM000664.2:g.178527073C= GRCh38
NC_000002.11:g.179391800C= , CM000664.1:g.179391800C= GRCh37
NC_000002.10:g.179100046C= NCBI36
NG_011618.3:g.308730G= , LRG_391:g.308730G=
NG_051363.1:g.9247C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.100211G= (TTN) ENSP00000343764.6:p.Ser33404=
ENST00000342175.11:c.81296G= (TTN) ENSP00000340554.6:p.Ser27099=
ENST00000359218.10:c.81095G= (TTN) ENSP00000352154.5:p.Ser27032=
ENST00000342175.10:c.81296G= (TTN) ENSP00000340554.6:p.Ser27099=
ENST00000342992.10:c.100211G= (TTN) ENSP00000343764.6:p.Ser33404=
ENST00000359218.9:c.81095G= (TTN) ENSP00000352154.5:p.Ser27032=
ENST00000460472.6:c.80720G= (TTN) ENSP00000434586.1:p.Ser26907=
ENST00000589042.5:c.107915G= (TTN) MANE Select ENSP00000467141.1:p.Ser35972=
ENST00000591111.5:c.102992G= (TTN) ENSP00000465570.1:p.Ser34331=
ENST00000615779.4:c.102992G= (TTN) ENSP00000483597.1:p.Ser34331=
NM_001256850.1:c.102992G= (TTN) NP_001243779.1:p.Ser34331=
NM_001267550.2:c.107915G= (TTN) MANE Select NP_001254479.2:p.Ser35972=
NM_003319.4:c.80720G= (TTN) NP_003310.4:p.Ser26907=
NM_133378.4:c.100211G= (TTN) NP_596869.4:p.Ser33404=
NM_133432.3:c.81095G= (TTN) NP_597676.3:p.Ser27032=
NM_133437.4:c.81296G= (TTN) NP_597681.4:p.Ser27099=
NR_038271.1:n.446+3437C= (TTN-AS1)
NR_038272.1:n.219+3437C= (TTN-AS1)
XM_011511729.1:c.107012G= (TTN) XP_011510031.1:p.Ser35671=
XM_011511730.1:c.80906G= (TTN) XP_011510032.1:p.Ser26969=
XM_011511731.1:c.80765G= (TTN) XP_011510033.1:p.Ser26922=
XM_017004819.1:c.106808G= (TTN) XP_016860308.1:p.Ser35603=
XM_017004820.1:c.102206G= (TTN) XP_016860309.1:p.Ser34069=
XM_017004821.1:c.102203G= (TTN) XP_016860310.1:p.Ser34068=
XM_017004822.1:c.99245G= (TTN) XP_016860311.1:p.Ser33082=
XM_017004823.1:c.80861G= (TTN) XP_016860312.1:p.Ser26954=
XM_024453094.1:c.102356G= (TTN) XP_024308862.1:p.Ser34119=
XM_024453095.1:c.102353G= (TTN) XP_024308863.1:p.Ser34118=
XM_024453096.1:c.101786G= (TTN) XP_024308864.1:p.Ser33929=
XM_024453097.1:c.99128G= (TTN) XP_024308865.1:p.Ser33043=
XM_024453098.1:c.99047G= (TTN) XP_024308866.1:p.Ser33016=
XM_024453099.1:c.80810G= (TTN) XP_024308867.1:p.Ser26937=
XM_024453100.1:c.70664G= (TTN) XP_024308868.1:p.Ser23555=