Canonical Allele Identifier: CA430276477
Gene: TTN HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.179495894T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178631167T>A , CM000664.2:g.178631167T>A GRCh38
NC_000002.11:g.179495894T>A , CM000664.1:g.179495894T>A GRCh37
NC_000002.10:g.179204139T>A NCBI36
NG_011618.3:g.204636A>T , LRG_391:g.204636A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.36177A>T ENSP00000343764.6:p.Pro12059=
ENST00000342175.11:c.17262A>T ENSP00000340554.6:p.Pro5754=
ENST00000359218.10:c.17061A>T ENSP00000352154.5:p.Pro5687=
ENST00000342175.10:c.17262A>T ENSP00000340554.6:p.Pro5754=
ENST00000342992.10:c.36177A>T ENSP00000343764.6:p.Pro12059=
ENST00000359218.9:c.17061A>T ENSP00000352154.5:p.Pro5687=
ENST00000460472.6:c.16686A>T ENSP00000434586.1:p.Pro5562=
ENST00000589042.5:c.43881A>T MANE Select ENSP00000467141.1:p.Pro14627=
ENST00000591111.5:c.38958A>T ENSP00000465570.1:p.Pro12986=
ENST00000615779.4:c.38958A>T ENSP00000483597.1:p.Pro12986=
NM_001256850.1:c.38958A>T NP_001243779.1:p.Pro12986=
NM_001267550.2:c.43881A>T MANE Select NP_001254479.2:p.Pro14627=
NM_003319.4:c.16686A>T NP_003310.4:p.Pro5562=
NM_133378.4:c.36177A>T NP_596869.4:p.Pro12059=
NM_133432.3:c.17061A>T NP_597676.3:p.Pro5687=
NM_133437.4:c.17262A>T NP_597681.4:p.Pro5754=
XM_011511729.1:c.42978A>T XP_011510031.1:p.Pro14326=
XM_011511730.1:c.16872A>T XP_011510032.1:p.Pro5624=
XM_011511731.1:c.16731A>T XP_011510033.1:p.Pro5577=
XM_017004819.1:c.42774A>T XP_016860308.1:p.Pro14258=
XM_017004820.1:c.38172A>T XP_016860309.1:p.Pro12724=
XM_017004821.1:c.38169A>T XP_016860310.1:p.Pro12723=
XM_017004822.1:c.35211A>T XP_016860311.1:p.Pro11737=
XM_017004823.1:c.16827A>T XP_016860312.1:p.Pro5609=
XM_024453094.1:c.38322A>T XP_024308862.1:p.Pro12774=
XM_024453095.1:c.38319A>T XP_024308863.1:p.Pro12773=
XM_024453096.1:c.37752A>T XP_024308864.1:p.Pro12584=
XM_024453097.1:c.35094A>T XP_024308865.1:p.Pro11698=
XM_024453098.1:c.35013A>T XP_024308866.1:p.Pro11671=
XM_024453099.1:c.16776A>T XP_024308867.1:p.Pro5592=
XM_024453100.1:c.6630A>T XP_024308868.1:p.Pro2210=