Canonical Allele Identifier: CA1310549451

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178614635T= , CM000664.2:g.178614635T=	GRCh38
NC_000002.11:g.179479362T= , CM000664.1:g.179479362T=	GRCh37
NC_000002.10:g.179187607T=	NCBI36
NG_011618.3:g.221168A= , LRG_391:g.221168A=
NG_051363.1:g.96809T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.41175A= (TTN)	ENSP00000343764.6:p.Thr13725=
ENST00000342175.11:c.22260A= (TTN)	ENSP00000340554.6:p.Thr7420=
ENST00000359218.10:c.22059A= (TTN)	ENSP00000352154.5:p.Thr7353=
ENST00000342175.10:c.22260A= (TTN)	ENSP00000340554.6:p.Thr7420=
ENST00000342992.10:c.41175A= (TTN)	ENSP00000343764.6:p.Thr13725=
ENST00000359218.9:c.22059A= (TTN)	ENSP00000352154.5:p.Thr7353=
ENST00000460472.6:c.21684A= (TTN)	ENSP00000434586.1:p.Thr7228=
ENST00000589042.5:c.48879A= (TTN) MANE Select	ENSP00000467141.1:p.Thr16293=
ENST00000591111.5:c.43956A= (TTN)	ENSP00000465570.1:p.Thr14652=
ENST00000615779.4:c.43956A= (TTN)	ENSP00000483597.1:p.Thr14652=
NM_001256850.1:c.43956A= (TTN)	NP_001243779.1:p.Thr14652=
NM_001267550.2:c.48879A= (TTN) MANE Select	NP_001254479.2:p.Thr16293=
NM_003319.4:c.21684A= (TTN)	NP_003310.4:p.Thr7228=
NM_133378.4:c.41175A= (TTN)	NP_596869.4:p.Thr13725=
NM_133432.3:c.22059A= (TTN)	NP_597676.3:p.Thr7353=
NM_133437.4:c.22260A= (TTN)	NP_597681.4:p.Thr7420=
NR_038271.1:n.1383T= (TTN-AS1)
XM_011511729.1:c.47976A= (TTN)	XP_011510031.1:p.Thr15992=
XM_011511730.1:c.21870A= (TTN)	XP_011510032.1:p.Thr7290=
XM_011511731.1:c.21729A= (TTN)	XP_011510033.1:p.Thr7243=
XM_017004819.1:c.47772A= (TTN)	XP_016860308.1:p.Thr15924=
XM_017004820.1:c.43170A= (TTN)	XP_016860309.1:p.Thr14390=
XM_017004821.1:c.43167A= (TTN)	XP_016860310.1:p.Thr14389=
XM_017004822.1:c.40209A= (TTN)	XP_016860311.1:p.Thr13403=
XM_017004823.1:c.21825A= (TTN)	XP_016860312.1:p.Thr7275=
XM_024453094.1:c.43320A= (TTN)	XP_024308862.1:p.Thr14440=
XM_024453095.1:c.43317A= (TTN)	XP_024308863.1:p.Thr14439=
XM_024453096.1:c.42750A= (TTN)	XP_024308864.1:p.Thr14250=
XM_024453097.1:c.40092A= (TTN)	XP_024308865.1:p.Thr13364=
XM_024453098.1:c.40011A= (TTN)	XP_024308866.1:p.Thr13337=
XM_024453099.1:c.21774A= (TTN)	XP_024308867.1:p.Thr7258=
XM_024453100.1:c.11628A= (TTN)	XP_024308868.1:p.Thr3876=