Canonical Allele Identifier: CA2580064784

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178587779_178587781delinsCCA , CM000664.2:g.178587779_178587781delinsCCA	GRCh38
NC_000002.11:g.179452506_179452508delinsCCA , CM000664.1:g.179452506_179452508delinsCCA	GRCh37
NC_000002.10:g.179160752_179160754delinsCCA	NCBI36
NG_011618.3:g.248022_248024delinsTGG , LRG_391:g.248022_248024delinsTGG
NG_051363.1:g.69953_69955delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.63528_63530delinsTGG (TTN) MANE Select	NP_001254479.2:p.Leu21176_Asp21177delinsPheGly
ENST00000589042.5:c.63528_63530delinsTGG (TTN) MANE Select	ENSP00000467141.1:p.Leu21176_Asp21177delinsPheGly
NM_001256850.1:c.58605_58607delinsTGG (TTN)	NP_001243779.1:p.Leu19535_Asp19536delinsPheGly
NM_003319.4:c.36333_36335delinsTGG (TTN)	NP_003310.4:p.Leu12111_Asp12112delinsPheGly
NM_133378.4:c.55824_55826delinsTGG (TTN)	NP_596869.4:p.Leu18608_Asp18609delinsPheGly
NM_133432.3:c.36708_36710delinsTGG (TTN)	NP_597676.3:p.Leu12236_Asp12237delinsPheGly
NM_133437.4:c.36909_36911delinsTGG (TTN)	NP_597681.4:p.Leu12303_Asp12304delinsPheGly
NR_038271.1:n.597-9817_597-9815delinsCCA (TTN-AS1)
NR_038272.1:n.3188+2786_3188+2788delinsCCA (TTN-AS1)
ENST00000342175.10:c.36909_36911delinsTGG (TTN)	ENSP00000340554.6:p.Leu12303_Asp12304delinsPheGly
ENST00000342175.11:c.36909_36911delinsTGG (TTN)	ENSP00000340554.6:p.Leu12303_Asp12304delinsPheGly
ENST00000342992.10:c.55824_55826delinsTGG (TTN)	ENSP00000343764.6:p.Leu18608_Asp18609delinsPheGly
ENST00000342992.11:c.55824_55826delinsTGG (TTN)	ENSP00000343764.6:p.Leu18608_Asp18609delinsPheGly
ENST00000359218.10:c.36708_36710delinsTGG (TTN)	ENSP00000352154.5:p.Leu12236_Asp12237delinsPheGly
ENST00000359218.9:c.36708_36710delinsTGG (TTN)	ENSP00000352154.5:p.Leu12236_Asp12237delinsPheGly
ENST00000460472.6:c.36333_36335delinsTGG (TTN)	ENSP00000434586.1:p.Leu12111_Asp12112delinsPheGly
ENST00000591111.5:c.58605_58607delinsTGG (TTN)	ENSP00000465570.1:p.Leu19535_Asp19536delinsPheGly
ENST00000615779.4:c.58605_58607delinsTGG (TTN)	ENSP00000483597.1:p.Leu19535_Asp19536delinsPheGly
XM_011511729.1:c.62625_62627delinsTGG (TTN)	XP_011510031.1:p.Leu20875_Asp20876delinsPheGly
XM_011511730.1:c.36519_36521delinsTGG (TTN)	XP_011510032.1:p.Leu12173_Asp12174delinsPheGly
XM_011511731.1:c.36378_36380delinsTGG (TTN)	XP_011510033.1:p.Leu12126_Asp12127delinsPheGly
XM_017004819.1:c.62421_62423delinsTGG (TTN)	XP_016860308.1:p.Leu20807_Asp20808delinsPheGly
XM_017004820.1:c.57819_57821delinsTGG (TTN)	XP_016860309.1:p.Leu19273_Asp19274delinsPheGly
XM_017004821.1:c.57816_57818delinsTGG (TTN)	XP_016860310.1:p.Leu19272_Asp19273delinsPheGly
XM_017004822.1:c.54858_54860delinsTGG (TTN)	XP_016860311.1:p.Leu18286_Asp18287delinsPheGly
XM_017004823.1:c.36474_36476delinsTGG (TTN)	XP_016860312.1:p.Leu12158_Asp12159delinsPheGly
XM_024453094.1:c.57969_57971delinsTGG (TTN)	XP_024308862.1:p.Leu19323_Asp19324delinsPheGly
XM_024453095.1:c.57966_57968delinsTGG (TTN)	XP_024308863.1:p.Leu19322_Asp19323delinsPheGly
XM_024453096.1:c.57399_57401delinsTGG (TTN)	XP_024308864.1:p.Leu19133_Asp19134delinsPheGly
XM_024453097.1:c.54741_54743delinsTGG (TTN)	XP_024308865.1:p.Leu18247_Asp18248delinsPheGly
XM_024453098.1:c.54660_54662delinsTGG (TTN)	XP_024308866.1:p.Leu18220_Asp18221delinsPheGly
XM_024453099.1:c.36423_36425delinsTGG (TTN)	XP_024308867.1:p.Leu12141_Asp12142delinsPheGly
XM_024453100.1:c.26277_26279delinsTGG (TTN)	XP_024308868.1:p.Leu8759_Asp8760delinsPheGly