Canonical Allele Identifier: CA430113562
Gene: TTN HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.179495053A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630326A>C , CM000664.2:g.178630326A>C GRCh38
NC_000002.11:g.179495053A>C , CM000664.1:g.179495053A>C GRCh37
NC_000002.10:g.179203298A>C NCBI36
NG_011618.3:g.205477T>G , LRG_391:g.205477T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36492T>G ENSP00000343764.6:p.Val12164=
ENST00000342175.11:c.17577T>G ENSP00000340554.6:p.Val5859=
ENST00000359218.10:c.17376T>G ENSP00000352154.5:p.Val5792=
ENST00000342175.10:c.17577T>G ENSP00000340554.6:p.Val5859=
ENST00000342992.10:c.36492T>G ENSP00000343764.6:p.Val12164=
ENST00000359218.9:c.17376T>G ENSP00000352154.5:p.Val5792=
ENST00000460472.6:c.17001T>G ENSP00000434586.1:p.Val5667=
ENST00000589042.5:c.44196T>G MANE Select ENSP00000467141.1:p.Val14732=
ENST00000591111.5:c.39273T>G ENSP00000465570.1:p.Val13091=
ENST00000615779.4:c.39273T>G ENSP00000483597.1:p.Val13091=
NM_001256850.1:c.39273T>G NP_001243779.1:p.Val13091=
NM_001267550.2:c.44196T>G MANE Select NP_001254479.2:p.Val14732=
NM_003319.4:c.17001T>G NP_003310.4:p.Val5667=
NM_133378.4:c.36492T>G NP_596869.4:p.Val12164=
NM_133432.3:c.17376T>G NP_597676.3:p.Val5792=
NM_133437.4:c.17577T>G NP_597681.4:p.Val5859=
XM_011511729.1:c.43293T>G XP_011510031.1:p.Val14431=
XM_011511730.1:c.17187T>G XP_011510032.1:p.Val5729=
XM_011511731.1:c.17046T>G XP_011510033.1:p.Val5682=
XM_017004819.1:c.43089T>G XP_016860308.1:p.Val14363=
XM_017004820.1:c.38487T>G XP_016860309.1:p.Val12829=
XM_017004821.1:c.38484T>G XP_016860310.1:p.Val12828=
XM_017004822.1:c.35526T>G XP_016860311.1:p.Val11842=
XM_017004823.1:c.17142T>G XP_016860312.1:p.Val5714=
XM_024453094.1:c.38637T>G XP_024308862.1:p.Val12879=
XM_024453095.1:c.38634T>G XP_024308863.1:p.Val12878=
XM_024453096.1:c.38067T>G XP_024308864.1:p.Val12689=
XM_024453097.1:c.35409T>G XP_024308865.1:p.Val11803=
XM_024453098.1:c.35328T>G XP_024308866.1:p.Val11776=
XM_024453099.1:c.17091T>G XP_024308867.1:p.Val5697=
XM_024453100.1:c.6945T>G XP_024308868.1:p.Val2315=