Canonical Allele Identifier: CA349547838
Community Standard Title: NM_001267550.2(TTN):c.32452G>T (p.Glu10818Ter)
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178685271C>A , CM000664.2:g.178685271C>A GRCh38
NC_000002.11:g.179549998C>A , CM000664.1:g.179549998C>A GRCh37
NC_000002.10:g.179258243C>A NCBI36
NG_011618.3:g.150532G>T , LRG_391:g.150532G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001267550.2:c.32452G>T MANE Select NP_001254479.2:p.Glu10818Ter
ENST00000589042.5:c.32452G>T MANE Select ENSP00000467141.1:p.Glu10818Ter
NM_001256850.1:c.31501G>T NP_001243779.1:p.Glu10501Ter
NM_003319.4:c.13283-42954G>T NP_003310.4:n.13283-42954G>T
NM_133378.4:c.28720G>T NP_596869.4:p.Glu9574Ter
NM_133432.3:c.13658-42954G>T NP_597676.3:n.13658-42954G>T
NM_133437.4:c.13859-42954G>T NP_597681.4:n.13859-42954G>T
ENST00000342175.10:c.13859-42954G>T ENSP00000340554.6:n.13859-42954G>T
ENST00000342175.11:c.13859-42954G>T ENSP00000340554.6:n.13859-42954G>T
ENST00000342992.10:c.28720G>T ENSP00000343764.6:p.Glu9574Ter
ENST00000342992.11:c.28720G>T ENSP00000343764.6:p.Glu9574Ter
ENST00000359218.10:c.13658-42954G>T ENSP00000352154.5:n.13658-42954G>T
ENST00000359218.9:c.13658-42954G>T ENSP00000352154.5:n.13658-42954G>T
ENST00000414766.5:c.1730-2368G>T ENSP00000401501.1:n.1730-2368G>T
ENST00000460472.6:c.13283-42954G>T ENSP00000434586.1:n.13283-42954G>T
ENST00000591111.5:c.31501G>T ENSP00000465570.1:p.Glu10501Ter
ENST00000615779.4:c.31501G>T ENSP00000483597.1:p.Glu10501Ter
XM_011511729.1:c.31549G>T XP_011510031.1:p.Glu10517Ter
XM_011511730.1:c.13469-42954G>T XP_011510032.1:n.13469-42954G>T
XM_011511731.1:c.13328-42954G>T XP_011510033.1:n.13328-42954G>T
XM_017004819.1:c.31504G>T XP_016860308.1:p.Glu10502Ter
XM_017004820.1:c.28723G>T XP_016860309.1:p.Glu9575Ter
XM_017004821.1:c.28720G>T XP_016860310.1:p.Glu9574Ter
XM_017004822.1:c.31148-2368G>T XP_016860311.1:n.31148-2368G>T
XM_017004823.1:c.13424-42954G>T XP_016860312.1:n.13424-42954G>T
XM_024453094.1:c.31504G>T XP_024308862.1:p.Glu10502Ter
XM_024453095.1:c.31504G>T XP_024308863.1:p.Glu10502Ter
XM_024453096.1:c.31504G>T XP_024308864.1:p.Glu10502Ter
XM_024453097.1:c.30899-1980G>T XP_024308865.1:n.30899-1980G>T
XM_024453098.1:c.30899-2368G>T XP_024308866.1:n.30899-2368G>T
XM_024453099.1:c.13424-42954G>T XP_024308867.1:n.13424-42954G>T