Canonical Allele Identifier: CA1310532957

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178574894G= , CM000664.2:g.178574894G= GRCh38
NC_000002.11:g.179439621G= , CM000664.1:g.179439621G= GRCh37
NC_000002.10:g.179147867G= NCBI36
NG_011618.3:g.260909C= , LRG_391:g.260909C=
NG_051363.1:g.57068G=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.63534C= (TTN) ENSP00000343764.6:p.Phe21178=
ENST00000342175.11:c.44619C= (TTN) ENSP00000340554.6:p.Phe14873=
ENST00000359218.10:c.44418C= (TTN) ENSP00000352154.5:p.Phe14806=
ENST00000342175.10:c.44619C= (TTN) ENSP00000340554.6:p.Phe14873=
ENST00000342992.10:c.63534C= (TTN) ENSP00000343764.6:p.Phe21178=
ENST00000359218.9:c.44418C= (TTN) ENSP00000352154.5:p.Phe14806=
ENST00000460472.6:c.44043C= (TTN) ENSP00000434586.1:p.Phe14681=
ENST00000589042.5:c.71238C= (TTN) MANE Select ENSP00000467141.1:p.Phe23746=
ENST00000591111.5:c.66315C= (TTN) ENSP00000465570.1:p.Phe22105=
ENST00000615779.4:c.66315C= (TTN) ENSP00000483597.1:p.Phe22105=
NM_001256850.1:c.66315C= (TTN) NP_001243779.1:p.Phe22105=
NM_001267550.2:c.71238C= (TTN) MANE Select NP_001254479.2:p.Phe23746=
NM_003319.4:c.44043C= (TTN) NP_003310.4:p.Phe14681=
NM_133378.4:c.63534C= (TTN) NP_596869.4:p.Phe21178=
NM_133432.3:c.44418C= (TTN) NP_597676.3:p.Phe14806=
NM_133437.4:c.44619C= (TTN) NP_597681.4:p.Phe14873=
NR_038271.1:n.596+3445G= (TTN-AS1)
NR_038272.1:n.2044-7678G= (TTN-AS1)
XM_011511729.1:c.70335C= (TTN) XP_011510031.1:p.Phe23445=
XM_011511730.1:c.44229C= (TTN) XP_011510032.1:p.Phe14743=
XM_011511731.1:c.44088C= (TTN) XP_011510033.1:p.Phe14696=
XM_017004819.1:c.70131C= (TTN) XP_016860308.1:p.Phe23377=
XM_017004820.1:c.65529C= (TTN) XP_016860309.1:p.Phe21843=
XM_017004821.1:c.65526C= (TTN) XP_016860310.1:p.Phe21842=
XM_017004822.1:c.62568C= (TTN) XP_016860311.1:p.Phe20856=
XM_017004823.1:c.44184C= (TTN) XP_016860312.1:p.Phe14728=
XM_024453094.1:c.65679C= (TTN) XP_024308862.1:p.Phe21893=
XM_024453095.1:c.65676C= (TTN) XP_024308863.1:p.Phe21892=
XM_024453096.1:c.65109C= (TTN) XP_024308864.1:p.Phe21703=
XM_024453097.1:c.62451C= (TTN) XP_024308865.1:p.Phe20817=
XM_024453098.1:c.62370C= (TTN) XP_024308866.1:p.Phe20790=
XM_024453099.1:c.44133C= (TTN) XP_024308867.1:p.Phe14711=
XM_024453100.1:c.33987C= (TTN) XP_024308868.1:p.Phe11329=