Canonical Allele Identifier: CA1310520711

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178551067A= , CM000664.2:g.178551067A= GRCh38
NC_000002.11:g.179415794A= , CM000664.1:g.179415794A= GRCh37
NC_000002.10:g.179124040A= NCBI36
NG_011618.3:g.284736T= , LRG_391:g.284736T=
NG_051363.1:g.33241A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.83760T= (TTN) ENSP00000343764.6:p.Pro27920=
ENST00000342175.11:c.64845T= (TTN) ENSP00000340554.6:p.Pro21615=
ENST00000359218.10:c.64644T= (TTN) ENSP00000352154.5:p.Pro21548=
ENST00000342175.10:c.64845T= (TTN) ENSP00000340554.6:p.Pro21615=
ENST00000342992.10:c.83760T= (TTN) ENSP00000343764.6:p.Pro27920=
ENST00000359218.9:c.64644T= (TTN) ENSP00000352154.5:p.Pro21548=
ENST00000460472.6:c.64269T= (TTN) ENSP00000434586.1:p.Pro21423=
ENST00000589042.5:c.91464T= (TTN) MANE Select ENSP00000467141.1:p.Pro30488=
ENST00000591111.5:c.86541T= (TTN) ENSP00000465570.1:p.Pro28847=
ENST00000615779.4:c.86541T= (TTN) ENSP00000483597.1:p.Pro28847=
NM_001256850.1:c.86541T= (TTN) NP_001243779.1:p.Pro28847=
NM_001267550.2:c.91464T= (TTN) MANE Select NP_001254479.2:p.Pro30488=
NM_003319.4:c.64269T= (TTN) NP_003310.4:p.Pro21423=
NM_133378.4:c.83760T= (TTN) NP_596869.4:p.Pro27920=
NM_133432.3:c.64644T= (TTN) NP_597676.3:p.Pro21548=
NM_133437.4:c.64845T= (TTN) NP_597681.4:p.Pro21615=
NR_038271.1:n.447-20233A= (TTN-AS1)
NR_038272.1:n.2043+8706A= (TTN-AS1)
XM_011511729.1:c.90561T= (TTN) XP_011510031.1:p.Pro30187=
XM_011511730.1:c.64455T= (TTN) XP_011510032.1:p.Pro21485=
XM_011511731.1:c.64314T= (TTN) XP_011510033.1:p.Pro21438=
XM_017004819.1:c.90357T= (TTN) XP_016860308.1:p.Pro30119=
XM_017004820.1:c.85755T= (TTN) XP_016860309.1:p.Pro28585=
XM_017004821.1:c.85752T= (TTN) XP_016860310.1:p.Pro28584=
XM_017004822.1:c.82794T= (TTN) XP_016860311.1:p.Pro27598=
XM_017004823.1:c.64410T= (TTN) XP_016860312.1:p.Pro21470=
XM_024453094.1:c.85905T= (TTN) XP_024308862.1:p.Pro28635=
XM_024453095.1:c.85902T= (TTN) XP_024308863.1:p.Pro28634=
XM_024453096.1:c.85335T= (TTN) XP_024308864.1:p.Pro28445=
XM_024453097.1:c.82677T= (TTN) XP_024308865.1:p.Pro27559=
XM_024453098.1:c.82596T= (TTN) XP_024308866.1:p.Pro27532=
XM_024453099.1:c.64359T= (TTN) XP_024308867.1:p.Pro21453=
XM_024453100.1:c.54213T= (TTN) XP_024308868.1:p.Pro18071=