Canonical Allele Identifier: CA1310544524

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178602436T= , CM000664.2:g.178602436T=	GRCh38
NC_000002.11:g.179467163T= , CM000664.1:g.179467163T=	GRCh37
NC_000002.10:g.179175408T=	NCBI36
NG_011618.3:g.233367A= , LRG_391:g.233367A=
NG_051363.1:g.84610T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.47262A= (TTN)	ENSP00000343764.6:p.Val15754=
ENST00000342175.11:c.28347A= (TTN)	ENSP00000340554.6:p.Val9449=
ENST00000359218.10:c.28146A= (TTN)	ENSP00000352154.5:p.Val9382=
ENST00000342175.10:c.28347A= (TTN)	ENSP00000340554.6:p.Val9449=
ENST00000342992.10:c.47262A= (TTN)	ENSP00000343764.6:p.Val15754=
ENST00000359218.9:c.28146A= (TTN)	ENSP00000352154.5:p.Val9382=
ENST00000460472.6:c.27771A= (TTN)	ENSP00000434586.1:p.Val9257=
ENST00000589042.5:c.54966A= (TTN) MANE Select	ENSP00000467141.1:p.Val18322=
ENST00000591111.5:c.50043A= (TTN)	ENSP00000465570.1:p.Val16681=
ENST00000615779.4:c.50043A= (TTN)	ENSP00000483597.1:p.Val16681=
NM_001256850.1:c.50043A= (TTN)	NP_001243779.1:p.Val16681=
NM_001267550.2:c.54966A= (TTN) MANE Select	NP_001254479.2:p.Val18322=
NM_003319.4:c.27771A= (TTN)	NP_003310.4:p.Val9257=
NM_133378.4:c.47262A= (TTN)	NP_596869.4:p.Val15754=
NM_133432.3:c.28146A= (TTN)	NP_597676.3:p.Val9382=
NM_133437.4:c.28347A= (TTN)	NP_597681.4:p.Val9449=
NR_038271.1:n.682+4755T= (TTN-AS1)
NR_038272.1:n.3917+1769T= (TTN-AS1)
XM_011511729.1:c.54063A= (TTN)	XP_011510031.1:p.Val18021=
XM_011511730.1:c.27957A= (TTN)	XP_011510032.1:p.Val9319=
XM_011511731.1:c.27816A= (TTN)	XP_011510033.1:p.Val9272=
XM_017004819.1:c.53859A= (TTN)	XP_016860308.1:p.Val17953=
XM_017004820.1:c.49257A= (TTN)	XP_016860309.1:p.Val16419=
XM_017004821.1:c.49254A= (TTN)	XP_016860310.1:p.Val16418=
XM_017004822.1:c.46296A= (TTN)	XP_016860311.1:p.Val15432=
XM_017004823.1:c.27912A= (TTN)	XP_016860312.1:p.Val9304=
XM_024453094.1:c.49407A= (TTN)	XP_024308862.1:p.Val16469=
XM_024453095.1:c.49404A= (TTN)	XP_024308863.1:p.Val16468=
XM_024453096.1:c.48837A= (TTN)	XP_024308864.1:p.Val16279=
XM_024453097.1:c.46179A= (TTN)	XP_024308865.1:p.Val15393=
XM_024453098.1:c.46098A= (TTN)	XP_024308866.1:p.Val15366=
XM_024453099.1:c.27861A= (TTN)	XP_024308867.1:p.Val9287=
XM_024453100.1:c.17715A= (TTN)	XP_024308868.1:p.Val5905=