Canonical Allele Identifier: CA1310557941
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178635425G= , CM000664.2:g.178635425G= GRCh38
NC_000002.11:g.179500152G= , CM000664.1:g.179500152G= GRCh37
NC_000002.10:g.179208397G= NCBI36
NG_011618.3:g.200378C= , LRG_391:g.200378C=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.34180+15C= ENSP00000343764.6:n.34180+15C=
ENST00000342175.11:c.15265+15C= ENSP00000340554.6:n.15265+15C=
ENST00000359218.10:c.15064+15C= ENSP00000352154.5:n.15064+15C=
ENST00000342175.10:c.15265+15C= ENSP00000340554.6:n.15265+15C=
ENST00000342992.10:c.34180+15C= ENSP00000343764.6:n.34180+15C=
ENST00000359218.9:c.15064+15C= ENSP00000352154.5:n.15064+15C=
ENST00000460472.6:c.14689+15C= ENSP00000434586.1:n.14689+15C=
ENST00000589042.5:c.41884+15C= MANE Select ENSP00000467141.1:n.41884+15C=
ENST00000591111.5:c.36961+15C= ENSP00000465570.1:n.36961+15C=
ENST00000615779.4:c.36961+15C= ENSP00000483597.1:n.36961+15C=
NM_001256850.1:c.36961+15C= NP_001243779.1:n.36961+15C=
NM_001267550.2:c.41884+15C= MANE Select NP_001254479.2:n.41884+15C=
NM_003319.4:c.14689+15C= NP_003310.4:n.14689+15C=
NM_133378.4:c.34180+15C= NP_596869.4:n.34180+15C=
NM_133432.3:c.15064+15C= NP_597676.3:n.15064+15C=
NM_133437.4:c.15265+15C= NP_597681.4:n.15265+15C=
XM_011511729.1:c.40981+15C= XP_011510031.1:n.40981+15C=
XM_011511730.1:c.14875+15C= XP_011510032.1:n.14875+15C=
XM_011511731.1:c.14734+15C= XP_011510033.1:n.14734+15C=
XM_017004819.1:c.40777+15C= XP_016860308.1:n.40777+15C=
XM_017004820.1:c.36175+15C= XP_016860309.1:n.36175+15C=
XM_017004821.1:c.36172+15C= XP_016860310.1:n.36172+15C=
XM_017004822.1:c.33214+15C= XP_016860311.1:n.33214+15C=
XM_017004823.1:c.14830+15C= XP_016860312.1:n.14830+15C=
XM_024453094.1:c.36325+15C= XP_024308862.1:n.36325+15C=
XM_024453095.1:c.36322+15C= XP_024308863.1:n.36322+15C=
XM_024453096.1:c.35755+15C= XP_024308864.1:n.35755+15C=
XM_024453097.1:c.33097+15C= XP_024308865.1:n.33097+15C=
XM_024453098.1:c.33016+15C= XP_024308866.1:n.33016+15C=
XM_024453099.1:c.14779+15C= XP_024308867.1:n.14779+15C=
XM_024453100.1:c.4633+15C= XP_024308868.1:n.4633+15C=