Canonical Allele Identifier: CA1986305

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178539129G>A , CM000664.2:g.178539129G>A	GRCh38
NC_000002.11:g.179403856G>A , CM000664.1:g.179403856G>A	GRCh37
NC_000002.10:g.179112102G>A	NCBI36
NG_011618.3:g.296674C>T , LRG_391:g.296674C>T
NG_051363.1:g.21303G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.91102C>T (TTN)	ENSP00000343764.6:p.Arg30368Cys
ENST00000342175.11:c.72187C>T (TTN)	ENSP00000340554.6:p.Arg24063Cys
ENST00000359218.10:c.71986C>T (TTN)	ENSP00000352154.5:p.Arg23996Cys
ENST00000342175.10:c.72187C>T (TTN)	ENSP00000340554.6:p.Arg24063Cys
ENST00000342992.10:c.91102C>T (TTN)	ENSP00000343764.6:p.Arg30368Cys
ENST00000359218.9:c.71986C>T (TTN)	ENSP00000352154.5:p.Arg23996Cys
ENST00000460472.6:c.71611C>T (TTN)	ENSP00000434586.1:p.Arg23871Cys
ENST00000589042.5:c.98806C>T (TTN) MANE Select	ENSP00000467141.1:p.Arg32936Cys
ENST00000591111.5:c.93883C>T (TTN)	ENSP00000465570.1:p.Arg31295Cys
ENST00000615779.4:c.93883C>T (TTN)	ENSP00000483597.1:p.Arg31295Cys
NM_001256850.1:c.93883C>T (TTN)	NP_001243779.1:p.Arg31295Cys
NM_001267550.2:c.98806C>T (TTN) MANE Select	NP_001254479.2:p.Arg32936Cys
NM_003319.4:c.71611C>T (TTN)	NP_003310.4:p.Arg23871Cys
NM_133378.4:c.91102C>T (TTN)	NP_596869.4:p.Arg30368Cys
NM_133432.3:c.71986C>T (TTN)	NP_597676.3:p.Arg23996Cys
NM_133437.4:c.72187C>T (TTN)	NP_597681.4:p.Arg24063Cys
NR_038271.1:n.446+15493G>A (TTN-AS1)
NR_038272.1:n.1079G>A (TTN-AS1)
XM_011511729.1:c.97903C>T (TTN)	XP_011510031.1:p.Arg32635Cys
XM_011511730.1:c.71797C>T (TTN)	XP_011510032.1:p.Arg23933Cys
XM_011511731.1:c.71656C>T (TTN)	XP_011510033.1:p.Arg23886Cys
XM_017004819.1:c.97699C>T (TTN)	XP_016860308.1:p.Arg32567Cys
XM_017004820.1:c.93097C>T (TTN)	XP_016860309.1:p.Arg31033Cys
XM_017004821.1:c.93094C>T (TTN)	XP_016860310.1:p.Arg31032Cys
XM_017004822.1:c.90136C>T (TTN)	XP_016860311.1:p.Arg30046Cys
XM_017004823.1:c.71752C>T (TTN)	XP_016860312.1:p.Arg23918Cys
XM_024453094.1:c.93247C>T (TTN)	XP_024308862.1:p.Arg31083Cys
XM_024453095.1:c.93244C>T (TTN)	XP_024308863.1:p.Arg31082Cys
XM_024453096.1:c.92677C>T (TTN)	XP_024308864.1:p.Arg30893Cys
XM_024453097.1:c.90019C>T (TTN)	XP_024308865.1:p.Arg30007Cys
XM_024453098.1:c.89938C>T (TTN)	XP_024308866.1:p.Arg29980Cys
XM_024453099.1:c.71701C>T (TTN)	XP_024308867.1:p.Arg23901Cys
XM_024453100.1:c.61555C>T (TTN)	XP_024308868.1:p.Arg20519Cys