Canonical Allele Identifier: CA349656734
Gene: TTN HGNC NCBI

Linked Data

dbSNP Id: rs2060324191

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178635440C>T , CM000664.2:g.178635440C>T GRCh38
NC_000002.11:g.179500167C>T , CM000664.1:g.179500167C>T GRCh37
NC_000002.10:g.179208412C>T NCBI36
NG_011618.3:g.200363G>A , LRG_391:g.200363G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.34180G>A ENSP00000343764.6:p.Glu11394Lys
ENST00000342175.11:c.15265G>A ENSP00000340554.6:p.Glu5089Lys
ENST00000359218.10:c.15064G>A ENSP00000352154.5:p.Glu5022Lys
ENST00000342175.10:c.15265G>A ENSP00000340554.6:p.Glu5089Lys
ENST00000342992.10:c.34180G>A ENSP00000343764.6:p.Glu11394Lys
ENST00000359218.9:c.15064G>A ENSP00000352154.5:p.Glu5022Lys
ENST00000460472.6:c.14689G>A ENSP00000434586.1:p.Glu4897Lys
ENST00000589042.5:c.41884G>A MANE Select ENSP00000467141.1:p.Glu13962Lys
ENST00000591111.5:c.36961G>A ENSP00000465570.1:p.Glu12321Lys
ENST00000615779.4:c.36961G>A ENSP00000483597.1:p.Glu12321Lys
NM_001256850.1:c.36961G>A NP_001243779.1:p.Glu12321Lys
NM_001267550.2:c.41884G>A MANE Select NP_001254479.2:p.Glu13962Lys
NM_003319.4:c.14689G>A NP_003310.4:p.Glu4897Lys
NM_133378.4:c.34180G>A NP_596869.4:p.Glu11394Lys
NM_133432.3:c.15064G>A NP_597676.3:p.Glu5022Lys
NM_133437.4:c.15265G>A NP_597681.4:p.Glu5089Lys
XM_011511729.1:c.40981G>A XP_011510031.1:p.Glu13661Lys
XM_011511730.1:c.14875G>A XP_011510032.1:p.Glu4959Lys
XM_011511731.1:c.14734G>A XP_011510033.1:p.Glu4912Lys
XM_017004819.1:c.40777G>A XP_016860308.1:p.Glu13593Lys
XM_017004820.1:c.36175G>A XP_016860309.1:p.Glu12059Lys
XM_017004821.1:c.36172G>A XP_016860310.1:p.Glu12058Lys
XM_017004822.1:c.33214G>A XP_016860311.1:p.Glu11072Lys
XM_017004823.1:c.14830G>A XP_016860312.1:p.Glu4944Lys
XM_024453094.1:c.36325G>A XP_024308862.1:p.Glu12109Lys
XM_024453095.1:c.36322G>A XP_024308863.1:p.Glu12108Lys
XM_024453096.1:c.35755G>A XP_024308864.1:p.Glu11919Lys
XM_024453097.1:c.33097G>A XP_024308865.1:p.Glu11033Lys
XM_024453098.1:c.33016G>A XP_024308866.1:p.Glu11006Lys
XM_024453099.1:c.14779G>A XP_024308867.1:p.Glu4927Lys
XM_024453100.1:c.4633G>A XP_024308868.1:p.Glu1545Lys