Canonical Allele Identifier: CA430113548
Gene: TTN HGNC NCBI

Linked Data

dbSNP Id: rs1259077293

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630320G>A , CM000664.2:g.178630320G>A GRCh38
NC_000002.11:g.179495047G>A , CM000664.1:g.179495047G>A GRCh37
NC_000002.10:g.179203292G>A NCBI36
NG_011618.3:g.205483C>T , LRG_391:g.205483C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36498C>T ENSP00000343764.6:p.His12166=
ENST00000342175.11:c.17583C>T ENSP00000340554.6:p.His5861=
ENST00000359218.10:c.17382C>T ENSP00000352154.5:p.His5794=
ENST00000342175.10:c.17583C>T ENSP00000340554.6:p.His5861=
ENST00000342992.10:c.36498C>T ENSP00000343764.6:p.His12166=
ENST00000359218.9:c.17382C>T ENSP00000352154.5:p.His5794=
ENST00000460472.6:c.17007C>T ENSP00000434586.1:p.His5669=
ENST00000589042.5:c.44202C>T MANE Select ENSP00000467141.1:p.His14734=
ENST00000591111.5:c.39279C>T ENSP00000465570.1:p.His13093=
ENST00000615779.4:c.39279C>T ENSP00000483597.1:p.His13093=
NM_001256850.1:c.39279C>T NP_001243779.1:p.His13093=
NM_001267550.2:c.44202C>T MANE Select NP_001254479.2:p.His14734=
NM_003319.4:c.17007C>T NP_003310.4:p.His5669=
NM_133378.4:c.36498C>T NP_596869.4:p.His12166=
NM_133432.3:c.17382C>T NP_597676.3:p.His5794=
NM_133437.4:c.17583C>T NP_597681.4:p.His5861=
XM_011511729.1:c.43299C>T XP_011510031.1:p.His14433=
XM_011511730.1:c.17193C>T XP_011510032.1:p.His5731=
XM_011511731.1:c.17052C>T XP_011510033.1:p.His5684=
XM_017004819.1:c.43095C>T XP_016860308.1:p.His14365=
XM_017004820.1:c.38493C>T XP_016860309.1:p.His12831=
XM_017004821.1:c.38490C>T XP_016860310.1:p.His12830=
XM_017004822.1:c.35532C>T XP_016860311.1:p.His11844=
XM_017004823.1:c.17148C>T XP_016860312.1:p.His5716=
XM_024453094.1:c.38643C>T XP_024308862.1:p.His12881=
XM_024453095.1:c.38640C>T XP_024308863.1:p.His12880=
XM_024453096.1:c.38073C>T XP_024308864.1:p.His12691=
XM_024453097.1:c.35415C>T XP_024308865.1:p.His11805=
XM_024453098.1:c.35334C>T XP_024308866.1:p.His11778=
XM_024453099.1:c.17097C>T XP_024308867.1:p.His5699=
XM_024453100.1:c.6951C>T XP_024308868.1:p.His2317=