Canonical Allele Identifier: CA349646995
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178631166A>C , CM000664.2:g.178631166A>C GRCh38
NC_000002.11:g.179495893A>C , CM000664.1:g.179495893A>C GRCh37
NC_000002.10:g.179204138A>C NCBI36
NG_011618.3:g.204637T>G , LRG_391:g.204637T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.36178T>G ENSP00000343764.6:p.Ser12060Ala
ENST00000342175.11:c.17263T>G ENSP00000340554.6:p.Ser5755Ala
ENST00000359218.10:c.17062T>G ENSP00000352154.5:p.Ser5688Ala
ENST00000342175.10:c.17263T>G ENSP00000340554.6:p.Ser5755Ala
ENST00000342992.10:c.36178T>G ENSP00000343764.6:p.Ser12060Ala
ENST00000359218.9:c.17062T>G ENSP00000352154.5:p.Ser5688Ala
ENST00000460472.6:c.16687T>G ENSP00000434586.1:p.Ser5563Ala
ENST00000589042.5:c.43882T>G MANE Select ENSP00000467141.1:p.Ser14628Ala
ENST00000591111.5:c.38959T>G ENSP00000465570.1:p.Ser12987Ala
ENST00000615779.4:c.38959T>G ENSP00000483597.1:p.Ser12987Ala
NM_001256850.1:c.38959T>G NP_001243779.1:p.Ser12987Ala
NM_001267550.2:c.43882T>G MANE Select NP_001254479.2:p.Ser14628Ala
NM_003319.4:c.16687T>G NP_003310.4:p.Ser5563Ala
NM_133378.4:c.36178T>G NP_596869.4:p.Ser12060Ala
NM_133432.3:c.17062T>G NP_597676.3:p.Ser5688Ala
NM_133437.4:c.17263T>G NP_597681.4:p.Ser5755Ala
XM_011511729.1:c.42979T>G XP_011510031.1:p.Ser14327Ala
XM_011511730.1:c.16873T>G XP_011510032.1:p.Ser5625Ala
XM_011511731.1:c.16732T>G XP_011510033.1:p.Ser5578Ala
XM_017004819.1:c.42775T>G XP_016860308.1:p.Ser14259Ala
XM_017004820.1:c.38173T>G XP_016860309.1:p.Ser12725Ala
XM_017004821.1:c.38170T>G XP_016860310.1:p.Ser12724Ala
XM_017004822.1:c.35212T>G XP_016860311.1:p.Ser11738Ala
XM_017004823.1:c.16828T>G XP_016860312.1:p.Ser5610Ala
XM_024453094.1:c.38323T>G XP_024308862.1:p.Ser12775Ala
XM_024453095.1:c.38320T>G XP_024308863.1:p.Ser12774Ala
XM_024453096.1:c.37753T>G XP_024308864.1:p.Ser12585Ala
XM_024453097.1:c.35095T>G XP_024308865.1:p.Ser11699Ala
XM_024453098.1:c.35014T>G XP_024308866.1:p.Ser11672Ala
XM_024453099.1:c.16777T>G XP_024308867.1:p.Ser5593Ala
XM_024453100.1:c.6631T>G XP_024308868.1:p.Ser2211Ala