Canonical Allele Identifier: CA1310522012

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178552477G= , CM000664.2:g.178552477G= GRCh38
NC_000002.11:g.179417204G= , CM000664.1:g.179417204G= GRCh37
NC_000002.10:g.179125450G= NCBI36
NG_011618.3:g.283326C= , LRG_391:g.283326C=
NG_051363.1:g.34651G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.82719C= (TTN) ENSP00000343764.6:p.Val27573=
ENST00000342175.11:c.63804C= (TTN) ENSP00000340554.6:p.Val21268=
ENST00000359218.10:c.63603C= (TTN) ENSP00000352154.5:p.Val21201=
ENST00000342175.10:c.63804C= (TTN) ENSP00000340554.6:p.Val21268=
ENST00000342992.10:c.82719C= (TTN) ENSP00000343764.6:p.Val27573=
ENST00000359218.9:c.63603C= (TTN) ENSP00000352154.5:p.Val21201=
ENST00000460472.6:c.63228C= (TTN) ENSP00000434586.1:p.Val21076=
ENST00000589042.5:c.90423C= (TTN) MANE Select ENSP00000467141.1:p.Val30141=
ENST00000591111.5:c.85500C= (TTN) ENSP00000465570.1:p.Val28500=
ENST00000615779.4:c.85500C= (TTN) ENSP00000483597.1:p.Val28500=
NM_001256850.1:c.85500C= (TTN) NP_001243779.1:p.Val28500=
NM_001267550.2:c.90423C= (TTN) MANE Select NP_001254479.2:p.Val30141=
NM_003319.4:c.63228C= (TTN) NP_003310.4:p.Val21076=
NM_133378.4:c.82719C= (TTN) NP_596869.4:p.Val27573=
NM_133432.3:c.63603C= (TTN) NP_597676.3:p.Val21201=
NM_133437.4:c.63804C= (TTN) NP_597681.4:p.Val21268=
NR_038271.1:n.447-18823G= (TTN-AS1)
NR_038272.1:n.2043+10116G= (TTN-AS1)
XM_011511729.1:c.89520C= (TTN) XP_011510031.1:p.Val29840=
XM_011511730.1:c.63414C= (TTN) XP_011510032.1:p.Val21138=
XM_011511731.1:c.63273C= (TTN) XP_011510033.1:p.Val21091=
XM_017004819.1:c.89316C= (TTN) XP_016860308.1:p.Val29772=
XM_017004820.1:c.84714C= (TTN) XP_016860309.1:p.Val28238=
XM_017004821.1:c.84711C= (TTN) XP_016860310.1:p.Val28237=
XM_017004822.1:c.81753C= (TTN) XP_016860311.1:p.Val27251=
XM_017004823.1:c.63369C= (TTN) XP_016860312.1:p.Val21123=
XM_024453094.1:c.84864C= (TTN) XP_024308862.1:p.Val28288=
XM_024453095.1:c.84861C= (TTN) XP_024308863.1:p.Val28287=
XM_024453096.1:c.84294C= (TTN) XP_024308864.1:p.Val28098=
XM_024453097.1:c.81636C= (TTN) XP_024308865.1:p.Val27212=
XM_024453098.1:c.81555C= (TTN) XP_024308866.1:p.Val27185=
XM_024453099.1:c.63318C= (TTN) XP_024308867.1:p.Val21106=
XM_024453100.1:c.53172C= (TTN) XP_024308868.1:p.Val17724=