Canonical Allele Identifier: CA349507188

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178594035T>C , CM000664.2:g.178594035T>C GRCh38
NC_000002.11:g.179458762T>C , CM000664.1:g.179458762T>C GRCh37
NC_000002.10:g.179167008T>C NCBI36
NG_011618.3:g.241768A>G , LRG_391:g.241768A>G
NG_051363.1:g.76209T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.50654A>G (TTN) ENSP00000343764.6:p.Asp16885Gly
ENST00000342175.11:c.31739A>G (TTN) ENSP00000340554.6:p.Asp10580Gly
ENST00000359218.10:c.31538A>G (TTN) ENSP00000352154.5:p.Asp10513Gly
ENST00000342175.10:c.31739A>G (TTN) ENSP00000340554.6:p.Asp10580Gly
ENST00000342992.10:c.50654A>G (TTN) ENSP00000343764.6:p.Asp16885Gly
ENST00000359218.9:c.31538A>G (TTN) ENSP00000352154.5:p.Asp10513Gly
ENST00000460472.6:c.31163A>G (TTN) ENSP00000434586.1:p.Asp10388Gly
ENST00000589042.5:c.58358A>G (TTN) MANE Select ENSP00000467141.1:p.Asp19453Gly
ENST00000591111.5:c.53435A>G (TTN) ENSP00000465570.1:p.Asp17812Gly
ENST00000615779.4:c.53435A>G (TTN) ENSP00000483597.1:p.Asp17812Gly
NM_001256850.1:c.53435A>G (TTN) NP_001243779.1:p.Asp17812Gly
NM_001267550.2:c.58358A>G (TTN) MANE Select NP_001254479.2:p.Asp19453Gly
NM_003319.4:c.31163A>G (TTN) NP_003310.4:p.Asp10388Gly
NM_133378.4:c.50654A>G (TTN) NP_596869.4:p.Asp16885Gly
NM_133432.3:c.31538A>G (TTN) NP_597676.3:p.Asp10513Gly
NM_133437.4:c.31739A>G (TTN) NP_597681.4:p.Asp10580Gly
NR_038271.1:n.597-3561T>C (TTN-AS1)
NR_038272.1:n.3364+2721T>C (TTN-AS1)
XM_011511729.1:c.57455A>G (TTN) XP_011510031.1:p.Asp19152Gly
XM_011511730.1:c.31349A>G (TTN) XP_011510032.1:p.Asp10450Gly
XM_011511731.1:c.31208A>G (TTN) XP_011510033.1:p.Asp10403Gly
XM_017004819.1:c.57251A>G (TTN) XP_016860308.1:p.Asp19084Gly
XM_017004820.1:c.52649A>G (TTN) XP_016860309.1:p.Asp17550Gly
XM_017004821.1:c.52646A>G (TTN) XP_016860310.1:p.Asp17549Gly
XM_017004822.1:c.49688A>G (TTN) XP_016860311.1:p.Asp16563Gly
XM_017004823.1:c.31304A>G (TTN) XP_016860312.1:p.Asp10435Gly
XM_024453094.1:c.52799A>G (TTN) XP_024308862.1:p.Asp17600Gly
XM_024453095.1:c.52796A>G (TTN) XP_024308863.1:p.Asp17599Gly
XM_024453096.1:c.52229A>G (TTN) XP_024308864.1:p.Asp17410Gly
XM_024453097.1:c.49571A>G (TTN) XP_024308865.1:p.Asp16524Gly
XM_024453098.1:c.49490A>G (TTN) XP_024308866.1:p.Asp16497Gly
XM_024453099.1:c.31253A>G (TTN) XP_024308867.1:p.Asp10418Gly
XM_024453100.1:c.21107A>G (TTN) XP_024308868.1:p.Asp7036Gly