Canonical Allele Identifier: CA1310529830

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178567204G= , CM000664.2:g.178567204G= GRCh38
NC_000002.11:g.179431931G= , CM000664.1:g.179431931G= GRCh37
NC_000002.10:g.179140177G= NCBI36
NG_011618.3:g.268599C= , LRG_391:g.268599C=
NG_051363.1:g.49378G=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.71224C= (TTN) ENSP00000343764.6:p.Pro23742=
ENST00000342175.11:c.52309C= (TTN) ENSP00000340554.6:p.Pro17437=
ENST00000359218.10:c.52108C= (TTN) ENSP00000352154.5:p.Pro17370=
ENST00000342175.10:c.52309C= (TTN) ENSP00000340554.6:p.Pro17437=
ENST00000342992.10:c.71224C= (TTN) ENSP00000343764.6:p.Pro23742=
ENST00000359218.9:c.52108C= (TTN) ENSP00000352154.5:p.Pro17370=
ENST00000460472.6:c.51733C= (TTN) ENSP00000434586.1:p.Pro17245=
ENST00000589042.5:c.78928C= (TTN) MANE Select ENSP00000467141.1:p.Pro26310=
ENST00000591111.5:c.74005C= (TTN) ENSP00000465570.1:p.Pro24669=
ENST00000615779.4:c.74005C= (TTN) ENSP00000483597.1:p.Pro24669=
NM_001256850.1:c.74005C= (TTN) NP_001243779.1:p.Pro24669=
NM_001267550.2:c.78928C= (TTN) MANE Select NP_001254479.2:p.Pro26310=
NM_003319.4:c.51733C= (TTN) NP_003310.4:p.Pro17245=
NM_133378.4:c.71224C= (TTN) NP_596869.4:p.Pro23742=
NM_133432.3:c.52108C= (TTN) NP_597676.3:p.Pro17370=
NM_133437.4:c.52309C= (TTN) NP_597681.4:p.Pro17437=
NR_038271.1:n.447-4096G= (TTN-AS1)
NR_038272.1:n.2044-15368G= (TTN-AS1)
XM_011511729.1:c.78025C= (TTN) XP_011510031.1:p.Pro26009=
XM_011511730.1:c.51919C= (TTN) XP_011510032.1:p.Pro17307=
XM_011511731.1:c.51778C= (TTN) XP_011510033.1:p.Pro17260=
XM_017004819.1:c.77821C= (TTN) XP_016860308.1:p.Pro25941=
XM_017004820.1:c.73219C= (TTN) XP_016860309.1:p.Pro24407=
XM_017004821.1:c.73216C= (TTN) XP_016860310.1:p.Pro24406=
XM_017004822.1:c.70258C= (TTN) XP_016860311.1:p.Pro23420=
XM_017004823.1:c.51874C= (TTN) XP_016860312.1:p.Pro17292=
XM_024453094.1:c.73369C= (TTN) XP_024308862.1:p.Pro24457=
XM_024453095.1:c.73366C= (TTN) XP_024308863.1:p.Pro24456=
XM_024453096.1:c.72799C= (TTN) XP_024308864.1:p.Pro24267=
XM_024453097.1:c.70141C= (TTN) XP_024308865.1:p.Pro23381=
XM_024453098.1:c.70060C= (TTN) XP_024308866.1:p.Pro23354=
XM_024453099.1:c.51823C= (TTN) XP_024308867.1:p.Pro17275=
XM_024453100.1:c.41677C= (TTN) XP_024308868.1:p.Pro13893=