Canonical Allele Identifier: CA430276473
Gene: TTN HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.179495891G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178631164G>C , CM000664.2:g.178631164G>C GRCh38
NC_000002.11:g.179495891G>C , CM000664.1:g.179495891G>C GRCh37
NC_000002.10:g.179204136G>C NCBI36
NG_011618.3:g.204639C>G , LRG_391:g.204639C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.36180C>G ENSP00000343764.6:p.Ser12060=
ENST00000342175.11:c.17265C>G ENSP00000340554.6:p.Ser5755=
ENST00000359218.10:c.17064C>G ENSP00000352154.5:p.Ser5688=
ENST00000342175.10:c.17265C>G ENSP00000340554.6:p.Ser5755=
ENST00000342992.10:c.36180C>G ENSP00000343764.6:p.Ser12060=
ENST00000359218.9:c.17064C>G ENSP00000352154.5:p.Ser5688=
ENST00000460472.6:c.16689C>G ENSP00000434586.1:p.Ser5563=
ENST00000589042.5:c.43884C>G MANE Select ENSP00000467141.1:p.Ser14628=
ENST00000591111.5:c.38961C>G ENSP00000465570.1:p.Ser12987=
ENST00000615779.4:c.38961C>G ENSP00000483597.1:p.Ser12987=
NM_001256850.1:c.38961C>G NP_001243779.1:p.Ser12987=
NM_001267550.2:c.43884C>G MANE Select NP_001254479.2:p.Ser14628=
NM_003319.4:c.16689C>G NP_003310.4:p.Ser5563=
NM_133378.4:c.36180C>G NP_596869.4:p.Ser12060=
NM_133432.3:c.17064C>G NP_597676.3:p.Ser5688=
NM_133437.4:c.17265C>G NP_597681.4:p.Ser5755=
XM_011511729.1:c.42981C>G XP_011510031.1:p.Ser14327=
XM_011511730.1:c.16875C>G XP_011510032.1:p.Ser5625=
XM_011511731.1:c.16734C>G XP_011510033.1:p.Ser5578=
XM_017004819.1:c.42777C>G XP_016860308.1:p.Ser14259=
XM_017004820.1:c.38175C>G XP_016860309.1:p.Ser12725=
XM_017004821.1:c.38172C>G XP_016860310.1:p.Ser12724=
XM_017004822.1:c.35214C>G XP_016860311.1:p.Ser11738=
XM_017004823.1:c.16830C>G XP_016860312.1:p.Ser5610=
XM_024453094.1:c.38325C>G XP_024308862.1:p.Ser12775=
XM_024453095.1:c.38322C>G XP_024308863.1:p.Ser12774=
XM_024453096.1:c.37755C>G XP_024308864.1:p.Ser12585=
XM_024453097.1:c.35097C>G XP_024308865.1:p.Ser11699=
XM_024453098.1:c.35016C>G XP_024308866.1:p.Ser11672=
XM_024453099.1:c.16779C>G XP_024308867.1:p.Ser5593=
XM_024453100.1:c.6633C>G XP_024308868.1:p.Ser2211=