Canonical Allele Identifier: CA60950110

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178528547C>T , CM000664.2:g.178528547C>T	GRCh38
NC_000002.11:g.179393274C>T , CM000664.1:g.179393274C>T	GRCh37
NC_000002.10:g.179101520C>T	NCBI36
NG_011618.3:g.307256G>A , LRG_391:g.307256G>A
NG_051363.1:g.10721C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.107204G>A (TTN) MANE Select	NP_001254479.2:p.Trp35735Ter
ENST00000589042.5:c.107204G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp35735Ter
NM_001256850.1:c.102281G>A (TTN)	NP_001243779.1:p.Trp34094Ter
NM_003319.4:c.80009G>A (TTN)	NP_003310.4:p.Trp26670Ter
NM_133378.4:c.99500G>A (TTN)	NP_596869.4:p.Trp33167Ter
NM_133432.3:c.80384G>A (TTN)	NP_597676.3:p.Trp26795Ter
NM_133437.4:c.80585G>A (TTN)	NP_597681.4:p.Trp26862Ter
NR_038271.1:n.446+4911C>T (TTN-AS1)
NR_038272.1:n.219+4911C>T (TTN-AS1)
ENST00000342175.10:c.80585G>A (TTN)	ENSP00000340554.6:p.Trp26862Ter
ENST00000342175.11:c.80585G>A (TTN)	ENSP00000340554.6:p.Trp26862Ter
ENST00000342992.10:c.99500G>A (TTN)	ENSP00000343764.6:p.Trp33167Ter
ENST00000342992.11:c.99500G>A (TTN)	ENSP00000343764.6:p.Trp33167Ter
ENST00000359218.10:c.80384G>A (TTN)	ENSP00000352154.5:p.Trp26795Ter
ENST00000359218.9:c.80384G>A (TTN)	ENSP00000352154.5:p.Trp26795Ter
ENST00000460472.6:c.80009G>A (TTN)	ENSP00000434586.1:p.Trp26670Ter
ENST00000591111.5:c.102281G>A (TTN)	ENSP00000465570.1:p.Trp34094Ter
ENST00000615779.4:c.102281G>A (TTN)	ENSP00000483597.1:p.Trp34094Ter
XM_011511729.1:c.106301G>A (TTN)	XP_011510031.1:p.Trp35434Ter
XM_011511730.1:c.80195G>A (TTN)	XP_011510032.1:p.Trp26732Ter
XM_011511731.1:c.80054G>A (TTN)	XP_011510033.1:p.Trp26685Ter
XM_017004819.1:c.106097G>A (TTN)	XP_016860308.1:p.Trp35366Ter
XM_017004820.1:c.101495G>A (TTN)	XP_016860309.1:p.Trp33832Ter
XM_017004821.1:c.101492G>A (TTN)	XP_016860310.1:p.Trp33831Ter
XM_017004822.1:c.98534G>A (TTN)	XP_016860311.1:p.Trp32845Ter
XM_017004823.1:c.80150G>A (TTN)	XP_016860312.1:p.Trp26717Ter
XM_024453094.1:c.101645G>A (TTN)	XP_024308862.1:p.Trp33882Ter
XM_024453095.1:c.101642G>A (TTN)	XP_024308863.1:p.Trp33881Ter
XM_024453096.1:c.101075G>A (TTN)	XP_024308864.1:p.Trp33692Ter
XM_024453097.1:c.98417G>A (TTN)	XP_024308865.1:p.Trp32806Ter
XM_024453098.1:c.98336G>A (TTN)	XP_024308866.1:p.Trp32779Ter
XM_024453099.1:c.80099G>A (TTN)	XP_024308867.1:p.Trp26700Ter
XM_024453100.1:c.69953G>A (TTN)	XP_024308868.1:p.Trp23318Ter