Canonical Allele Identifier: CA349646945
Gene: TTN HGNC NCBI

Linked Data

dbSNP Id: rs1237863283

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178631156G>C , CM000664.2:g.178631156G>C GRCh38
NC_000002.11:g.179495883G>C , CM000664.1:g.179495883G>C GRCh37
NC_000002.10:g.179204128G>C NCBI36
NG_011618.3:g.204647C>G , LRG_391:g.204647C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.36188C>G ENSP00000343764.6:p.Ala12063Gly
ENST00000342175.11:c.17273C>G ENSP00000340554.6:p.Ala5758Gly
ENST00000359218.10:c.17072C>G ENSP00000352154.5:p.Ala5691Gly
ENST00000342175.10:c.17273C>G ENSP00000340554.6:p.Ala5758Gly
ENST00000342992.10:c.36188C>G ENSP00000343764.6:p.Ala12063Gly
ENST00000359218.9:c.17072C>G ENSP00000352154.5:p.Ala5691Gly
ENST00000460472.6:c.16697C>G ENSP00000434586.1:p.Ala5566Gly
ENST00000589042.5:c.43892C>G MANE Select ENSP00000467141.1:p.Ala14631Gly
ENST00000591111.5:c.38969C>G ENSP00000465570.1:p.Ala12990Gly
ENST00000615779.4:c.38969C>G ENSP00000483597.1:p.Ala12990Gly
NM_001256850.1:c.38969C>G NP_001243779.1:p.Ala12990Gly
NM_001267550.2:c.43892C>G MANE Select NP_001254479.2:p.Ala14631Gly
NM_003319.4:c.16697C>G NP_003310.4:p.Ala5566Gly
NM_133378.4:c.36188C>G NP_596869.4:p.Ala12063Gly
NM_133432.3:c.17072C>G NP_597676.3:p.Ala5691Gly
NM_133437.4:c.17273C>G NP_597681.4:p.Ala5758Gly
XM_011511729.1:c.42989C>G XP_011510031.1:p.Ala14330Gly
XM_011511730.1:c.16883C>G XP_011510032.1:p.Ala5628Gly
XM_011511731.1:c.16742C>G XP_011510033.1:p.Ala5581Gly
XM_017004819.1:c.42785C>G XP_016860308.1:p.Ala14262Gly
XM_017004820.1:c.38183C>G XP_016860309.1:p.Ala12728Gly
XM_017004821.1:c.38180C>G XP_016860310.1:p.Ala12727Gly
XM_017004822.1:c.35222C>G XP_016860311.1:p.Ala11741Gly
XM_017004823.1:c.16838C>G XP_016860312.1:p.Ala5613Gly
XM_024453094.1:c.38333C>G XP_024308862.1:p.Ala12778Gly
XM_024453095.1:c.38330C>G XP_024308863.1:p.Ala12777Gly
XM_024453096.1:c.37763C>G XP_024308864.1:p.Ala12588Gly
XM_024453097.1:c.35105C>G XP_024308865.1:p.Ala11702Gly
XM_024453098.1:c.35024C>G XP_024308866.1:p.Ala11675Gly
XM_024453099.1:c.16787C>G XP_024308867.1:p.Ala5596Gly
XM_024453100.1:c.6641C>G XP_024308868.1:p.Ala2214Gly