Canonical Allele Identifier: CA237746

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178560508T>C , CM000664.2:g.178560508T>C	GRCh38
NC_000002.11:g.179425235T>C , CM000664.1:g.179425235T>C	GRCh37
NC_000002.10:g.179133481T>C	NCBI36
NG_011618.3:g.275295A>G , LRG_391:g.275295A>G
NG_051363.1:g.42682T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.85624A>G (TTN) MANE Select	NP_001254479.2:p.Ile28542Val
ENST00000589042.5:c.85624A>G (TTN) MANE Select	ENSP00000467141.1:p.Ile28542Val
NM_001256850.1:c.80701A>G (TTN)	NP_001243779.1:p.Ile26901Val
NM_003319.4:c.58429A>G (TTN)	NP_003310.4:p.Ile19477Val
NM_133378.4:c.77920A>G (TTN)	NP_596869.4:p.Ile25974Val
NM_133432.3:c.58804A>G (TTN)	NP_597676.3:p.Ile19602Val
NM_133437.4:c.59005A>G (TTN)	NP_597681.4:p.Ile19669Val
NR_038271.1:n.447-10792T>C (TTN-AS1)
NR_038272.1:n.2043+18147T>C (TTN-AS1)
ENST00000342175.10:c.59005A>G (TTN)	ENSP00000340554.6:p.Ile19669Val
ENST00000342175.11:c.59005A>G (TTN)	ENSP00000340554.6:p.Ile19669Val
ENST00000342992.10:c.77920A>G (TTN)	ENSP00000343764.6:p.Ile25974Val
ENST00000342992.11:c.77920A>G (TTN)	ENSP00000343764.6:p.Ile25974Val
ENST00000359218.10:c.58804A>G (TTN)	ENSP00000352154.5:p.Ile19602Val
ENST00000359218.9:c.58804A>G (TTN)	ENSP00000352154.5:p.Ile19602Val
ENST00000460472.6:c.58429A>G (TTN)	ENSP00000434586.1:p.Ile19477Val
ENST00000591111.5:c.80701A>G (TTN)	ENSP00000465570.1:p.Ile26901Val
ENST00000615779.4:c.80701A>G (TTN)	ENSP00000483597.1:p.Ile26901Val
XM_011511729.1:c.84721A>G (TTN)	XP_011510031.1:p.Ile28241Val
XM_011511730.1:c.58615A>G (TTN)	XP_011510032.1:p.Ile19539Val
XM_011511731.1:c.58474A>G (TTN)	XP_011510033.1:p.Ile19492Val
XM_017004819.1:c.84517A>G (TTN)	XP_016860308.1:p.Ile28173Val
XM_017004820.1:c.79915A>G (TTN)	XP_016860309.1:p.Ile26639Val
XM_017004821.1:c.79912A>G (TTN)	XP_016860310.1:p.Ile26638Val
XM_017004822.1:c.76954A>G (TTN)	XP_016860311.1:p.Ile25652Val
XM_017004823.1:c.58570A>G (TTN)	XP_016860312.1:p.Ile19524Val
XM_024453094.1:c.80065A>G (TTN)	XP_024308862.1:p.Ile26689Val
XM_024453095.1:c.80062A>G (TTN)	XP_024308863.1:p.Ile26688Val
XM_024453096.1:c.79495A>G (TTN)	XP_024308864.1:p.Ile26499Val
XM_024453097.1:c.76837A>G (TTN)	XP_024308865.1:p.Ile25613Val
XM_024453098.1:c.76756A>G (TTN)	XP_024308866.1:p.Ile25586Val
XM_024453099.1:c.58519A>G (TTN)	XP_024308867.1:p.Ile19507Val
XM_024453100.1:c.48373A>G (TTN)	XP_024308868.1:p.Ile16125Val