Canonical Allele Identifier: CA1310511662

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530248T= , CM000664.2:g.178530248T=	GRCh38
NC_000002.11:g.179394975T= , CM000664.1:g.179394975T=	GRCh37
NC_000002.10:g.179103221T=	NCBI36
NG_011618.3:g.305555A= , LRG_391:g.305555A=
NG_051363.1:g.12422T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98663A= (TTN)	ENSP00000343764.6:p.Asp32888=
ENST00000342175.11:c.79748A= (TTN)	ENSP00000340554.6:p.Asp26583=
ENST00000359218.10:c.79547A= (TTN)	ENSP00000352154.5:p.Asp26516=
ENST00000342175.10:c.79748A= (TTN)	ENSP00000340554.6:p.Asp26583=
ENST00000342992.10:c.98663A= (TTN)	ENSP00000343764.6:p.Asp32888=
ENST00000359218.9:c.79547A= (TTN)	ENSP00000352154.5:p.Asp26516=
ENST00000460472.6:c.79172A= (TTN)	ENSP00000434586.1:p.Asp26391=
ENST00000589042.5:c.106367A= (TTN) MANE Select	ENSP00000467141.1:p.Asp35456=
ENST00000591111.5:c.101444A= (TTN)	ENSP00000465570.1:p.Asp33815=
ENST00000615779.4:c.101444A= (TTN)	ENSP00000483597.1:p.Asp33815=
NM_001256850.1:c.101444A= (TTN)	NP_001243779.1:p.Asp33815=
NM_001267550.2:c.106367A= (TTN) MANE Select	NP_001254479.2:p.Asp35456=
NM_003319.4:c.79172A= (TTN)	NP_003310.4:p.Asp26391=
NM_133378.4:c.98663A= (TTN)	NP_596869.4:p.Asp32888=
NM_133432.3:c.79547A= (TTN)	NP_597676.3:p.Asp26516=
NM_133437.4:c.79748A= (TTN)	NP_597681.4:p.Asp26583=
NR_038271.1:n.446+6612T= (TTN-AS1)
NR_038272.1:n.220-5484T= (TTN-AS1)
XM_011511729.1:c.105464A= (TTN)	XP_011510031.1:p.Asp35155=
XM_011511730.1:c.79358A= (TTN)	XP_011510032.1:p.Asp26453=
XM_011511731.1:c.79217A= (TTN)	XP_011510033.1:p.Asp26406=
XM_017004819.1:c.105260A= (TTN)	XP_016860308.1:p.Asp35087=
XM_017004820.1:c.100658A= (TTN)	XP_016860309.1:p.Asp33553=
XM_017004821.1:c.100655A= (TTN)	XP_016860310.1:p.Asp33552=
XM_017004822.1:c.97697A= (TTN)	XP_016860311.1:p.Asp32566=
XM_017004823.1:c.79313A= (TTN)	XP_016860312.1:p.Asp26438=
XM_024453094.1:c.100808A= (TTN)	XP_024308862.1:p.Asp33603=
XM_024453095.1:c.100805A= (TTN)	XP_024308863.1:p.Asp33602=
XM_024453096.1:c.100238A= (TTN)	XP_024308864.1:p.Asp33413=
XM_024453097.1:c.97580A= (TTN)	XP_024308865.1:p.Asp32527=
XM_024453098.1:c.97499A= (TTN)	XP_024308866.1:p.Asp32500=
XM_024453099.1:c.79262A= (TTN)	XP_024308867.1:p.Asp26421=
XM_024453100.1:c.69116A= (TTN)	XP_024308868.1:p.Asp23039=