Canonical Allele Identifier: CA309862
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178620484C>T , CM000664.2:g.178620484C>T GRCh38
NC_000002.11:g.179485211C>T , CM000664.1:g.179485211C>T GRCh37
NC_000002.10:g.179193456C>T NCBI36
NG_011618.3:g.215319G>A , LRG_391:g.215319G>A
NG_051363.1:g.102658C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.38333G>A ENSP00000343764.6:p.Arg12778His
ENST00000342175.11:c.19418G>A ENSP00000340554.6:p.Arg6473His
ENST00000359218.10:c.19217G>A ENSP00000352154.5:p.Arg6406His
ENST00000342175.10:c.19418G>A ENSP00000340554.6:p.Arg6473His
ENST00000342992.10:c.38333G>A ENSP00000343764.6:p.Arg12778His
ENST00000359218.9:c.19217G>A ENSP00000352154.5:p.Arg6406His
ENST00000460472.6:c.18842G>A ENSP00000434586.1:p.Arg6281His
ENST00000589042.5:c.46037G>A MANE Select ENSP00000467141.1:p.Arg15346His
ENST00000591111.5:c.41114G>A ENSP00000465570.1:p.Arg13705His
ENST00000615779.4:c.41114G>A ENSP00000483597.1:p.Arg13705His
NM_001256850.1:c.41114G>A NP_001243779.1:p.Arg13705His
NM_001267550.2:c.46037G>A MANE Select NP_001254479.2:p.Arg15346His
NM_003319.4:c.18842G>A NP_003310.4:p.Arg6281His
NM_133378.4:c.38333G>A NP_596869.4:p.Arg12778His
NM_133432.3:c.19217G>A NP_597676.3:p.Arg6406His
NM_133437.4:c.19418G>A NP_597681.4:p.Arg6473His
XM_011511729.1:c.45134G>A XP_011510031.1:p.Arg15045His
XM_011511730.1:c.19028G>A XP_011510032.1:p.Arg6343His
XM_011511731.1:c.18887G>A XP_011510033.1:p.Arg6296His
XM_017004819.1:c.44930G>A XP_016860308.1:p.Arg14977His
XM_017004820.1:c.40328G>A XP_016860309.1:p.Arg13443His
XM_017004821.1:c.40325G>A XP_016860310.1:p.Arg13442His
XM_017004822.1:c.37367G>A XP_016860311.1:p.Arg12456His
XM_017004823.1:c.18983G>A XP_016860312.1:p.Arg6328His
XM_024453094.1:c.40478G>A XP_024308862.1:p.Arg13493His
XM_024453095.1:c.40475G>A XP_024308863.1:p.Arg13492His
XM_024453096.1:c.39908G>A XP_024308864.1:p.Arg13303His
XM_024453097.1:c.37250G>A XP_024308865.1:p.Arg12417His
XM_024453098.1:c.37169G>A XP_024308866.1:p.Arg12390His
XM_024453099.1:c.18932G>A XP_024308867.1:p.Arg6311His
XM_024453100.1:c.8786G>A XP_024308868.1:p.Arg2929His