Canonical Allele Identifier: CA1310542975

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178598918C= , CM000664.2:g.178598918C=	GRCh38
NC_000002.11:g.179463645C= , CM000664.1:g.179463645C=	GRCh37
NC_000002.10:g.179171890C=	NCBI36
NG_011618.3:g.236885G= , LRG_391:g.236885G=
NG_051363.1:g.81092C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.56792G= (TTN) MANE Select	NP_001254479.2:p.Trp18931=
ENST00000589042.5:c.56792G= (TTN) MANE Select	ENSP00000467141.1:p.Trp18931=
NM_001256850.1:c.51869G= (TTN)	NP_001243779.1:p.Trp17290=
NM_003319.4:c.29597G= (TTN)	NP_003310.4:p.Trp9866=
NM_133378.4:c.49088G= (TTN)	NP_596869.4:p.Trp16363=
NM_133432.3:c.29972G= (TTN)	NP_597676.3:p.Trp9991=
NM_133437.4:c.30173G= (TTN)	NP_597681.4:p.Trp10058=
NR_038271.1:n.682+1237C= (TTN-AS1)
NR_038272.1:n.3568+245C= (TTN-AS1)
ENST00000342175.10:c.30173G= (TTN)	ENSP00000340554.6:p.Trp10058=
ENST00000342175.11:c.30173G= (TTN)	ENSP00000340554.6:p.Trp10058=
ENST00000342992.10:c.49088G= (TTN)	ENSP00000343764.6:p.Trp16363=
ENST00000342992.11:c.49088G= (TTN)	ENSP00000343764.6:p.Trp16363=
ENST00000359218.10:c.29972G= (TTN)	ENSP00000352154.5:p.Trp9991=
ENST00000359218.9:c.29972G= (TTN)	ENSP00000352154.5:p.Trp9991=
ENST00000460472.6:c.29597G= (TTN)	ENSP00000434586.1:p.Trp9866=
ENST00000591111.5:c.51869G= (TTN)	ENSP00000465570.1:p.Trp17290=
ENST00000615779.4:c.51869G= (TTN)	ENSP00000483597.1:p.Trp17290=
XM_011511729.1:c.55889G= (TTN)	XP_011510031.1:p.Trp18630=
XM_011511730.1:c.29783G= (TTN)	XP_011510032.1:p.Trp9928=
XM_011511731.1:c.29642G= (TTN)	XP_011510033.1:p.Trp9881=
XM_017004819.1:c.55685G= (TTN)	XP_016860308.1:p.Trp18562=
XM_017004820.1:c.51083G= (TTN)	XP_016860309.1:p.Trp17028=
XM_017004821.1:c.51080G= (TTN)	XP_016860310.1:p.Trp17027=
XM_017004822.1:c.48122G= (TTN)	XP_016860311.1:p.Trp16041=
XM_017004823.1:c.29738G= (TTN)	XP_016860312.1:p.Trp9913=
XM_024453094.1:c.51233G= (TTN)	XP_024308862.1:p.Trp17078=
XM_024453095.1:c.51230G= (TTN)	XP_024308863.1:p.Trp17077=
XM_024453096.1:c.50663G= (TTN)	XP_024308864.1:p.Trp16888=
XM_024453097.1:c.48005G= (TTN)	XP_024308865.1:p.Trp16002=
XM_024453098.1:c.47924G= (TTN)	XP_024308866.1:p.Trp15975=
XM_024453099.1:c.29687G= (TTN)	XP_024308867.1:p.Trp9896=
XM_024453100.1:c.19541G= (TTN)	XP_024308868.1:p.Trp6514=