Canonical Allele Identifier: CA1310558308
Community Standard Title: NM_001267550.2(TTN):c.41320G= (p.Val13774=)
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178636407C= , CM000664.2:g.178636407C= GRCh38
NC_000002.11:g.179501134C= , CM000664.1:g.179501134C= GRCh37
NC_000002.10:g.179209379C= NCBI36
NG_011618.3:g.199396G= , LRG_391:g.199396G=

Transcript Alleles

HGVS Amino-acid Change
NM_001267550.2:c.41320G= MANE Select NP_001254479.2:p.Val13774=
ENST00000589042.5:c.41320G= MANE Select ENSP00000467141.1:p.Val13774=
NM_001256850.1:c.36397G= NP_001243779.1:p.Val12133=
NM_003319.4:c.14125G= NP_003310.4:p.Val4709=
NM_133378.4:c.33616G= NP_596869.4:p.Val11206=
NM_133432.3:c.14500G= NP_597676.3:p.Val4834=
NM_133437.4:c.14701G= NP_597681.4:p.Val4901=
ENST00000342175.10:c.14701G= ENSP00000340554.6:p.Val4901=
ENST00000342175.11:c.14701G= ENSP00000340554.6:p.Val4901=
ENST00000342992.10:c.33616G= ENSP00000343764.6:p.Val11206=
ENST00000342992.11:c.33616G= ENSP00000343764.6:p.Val11206=
ENST00000359218.10:c.14500G= ENSP00000352154.5:p.Val4834=
ENST00000359218.9:c.14500G= ENSP00000352154.5:p.Val4834=
ENST00000460472.6:c.14125G= ENSP00000434586.1:p.Val4709=
ENST00000591111.5:c.36397G= ENSP00000465570.1:p.Val12133=
ENST00000615779.4:c.36397G= ENSP00000483597.1:p.Val12133=
XM_011511729.1:c.40417G= XP_011510031.1:p.Val13473=
XM_011511730.1:c.14311G= XP_011510032.1:p.Val4771=
XM_011511731.1:c.14170G= XP_011510033.1:p.Val4724=
XM_017004819.1:c.40213G= XP_016860308.1:p.Val13405=
XM_017004820.1:c.35611G= XP_016860309.1:p.Val11871=
XM_017004821.1:c.35608G= XP_016860310.1:p.Val11870=
XM_017004822.1:c.32650G= XP_016860311.1:p.Val10884=
XM_017004823.1:c.14266G= XP_016860312.1:p.Val4756=
XM_024453094.1:c.35761G= XP_024308862.1:p.Val11921=
XM_024453095.1:c.35758G= XP_024308863.1:p.Val11920=
XM_024453096.1:c.35191G= XP_024308864.1:p.Val11731=
XM_024453097.1:c.32533G= XP_024308865.1:p.Val10845=
XM_024453098.1:c.32452G= XP_024308866.1:p.Val10818=
XM_024453099.1:c.14215G= XP_024308867.1:p.Val4739=
XM_024453100.1:c.4069G= XP_024308868.1:p.Val1357=