Canonical Allele Identifier: CA61006255
Community Standard Title: NM_001267550.2(TTN):c.41641C>T (p.Arg13881Ter)
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178635683G>A , CM000664.2:g.178635683G>A GRCh38
NC_000002.11:g.179500410G>A , CM000664.1:g.179500410G>A GRCh37
NC_000002.10:g.179208655G>A NCBI36
NG_011618.3:g.200120C>T , LRG_391:g.200120C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001267550.2:c.41641C>T MANE Select NP_001254479.2:p.Arg13881Ter
ENST00000589042.5:c.41641C>T MANE Select ENSP00000467141.1:p.Arg13881Ter
NM_001256850.1:c.36718C>T NP_001243779.1:p.Arg12240Ter
NM_003319.4:c.14446C>T NP_003310.4:p.Arg4816Ter
NM_133378.4:c.33937C>T NP_596869.4:p.Arg11313Ter
NM_133432.3:c.14821C>T NP_597676.3:p.Arg4941Ter
NM_133437.4:c.15022C>T NP_597681.4:p.Arg5008Ter
ENST00000342175.10:c.15022C>T ENSP00000340554.6:p.Arg5008Ter
ENST00000342175.11:c.15022C>T ENSP00000340554.6:p.Arg5008Ter
ENST00000342992.10:c.33937C>T ENSP00000343764.6:p.Arg11313Ter
ENST00000342992.11:c.33937C>T ENSP00000343764.6:p.Arg11313Ter
ENST00000359218.10:c.14821C>T ENSP00000352154.5:p.Arg4941Ter
ENST00000359218.9:c.14821C>T ENSP00000352154.5:p.Arg4941Ter
ENST00000460472.6:c.14446C>T ENSP00000434586.1:p.Arg4816Ter
ENST00000591111.5:c.36718C>T ENSP00000465570.1:p.Arg12240Ter
ENST00000615779.4:c.36718C>T ENSP00000483597.1:p.Arg12240Ter
XM_011511729.1:c.40738C>T XP_011510031.1:p.Arg13580Ter
XM_011511730.1:c.14632C>T XP_011510032.1:p.Arg4878Ter
XM_011511731.1:c.14491C>T XP_011510033.1:p.Arg4831Ter
XM_017004819.1:c.40534C>T XP_016860308.1:p.Arg13512Ter
XM_017004820.1:c.35932C>T XP_016860309.1:p.Arg11978Ter
XM_017004821.1:c.35929C>T XP_016860310.1:p.Arg11977Ter
XM_017004822.1:c.32971C>T XP_016860311.1:p.Arg10991Ter
XM_017004823.1:c.14587C>T XP_016860312.1:p.Arg4863Ter
XM_024453094.1:c.36082C>T XP_024308862.1:p.Arg12028Ter
XM_024453095.1:c.36079C>T XP_024308863.1:p.Arg12027Ter
XM_024453096.1:c.35512C>T XP_024308864.1:p.Arg11838Ter
XM_024453097.1:c.32854C>T XP_024308865.1:p.Arg10952Ter
XM_024453098.1:c.32773C>T XP_024308866.1:p.Arg10925Ter
XM_024453099.1:c.14536C>T XP_024308867.1:p.Arg4846Ter
XM_024453100.1:c.4390C>T XP_024308868.1:p.Arg1464Ter