Canonical Allele Identifier: CA1310516546

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178539943C= , CM000664.2:g.178539943C=	GRCh38
NC_000002.11:g.179404670C= , CM000664.1:g.179404670C=	GRCh37
NC_000002.10:g.179112916C=	NCBI36
NG_011618.3:g.295860G= , LRG_391:g.295860G=
NG_051363.1:g.22117C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.90418G= (TTN)	ENSP00000343764.6:p.Glu30140=
ENST00000342175.11:c.71503G= (TTN)	ENSP00000340554.6:p.Glu23835=
ENST00000359218.10:c.71302G= (TTN)	ENSP00000352154.5:p.Glu23768=
ENST00000342175.10:c.71503G= (TTN)	ENSP00000340554.6:p.Glu23835=
ENST00000342992.10:c.90418G= (TTN)	ENSP00000343764.6:p.Glu30140=
ENST00000359218.9:c.71302G= (TTN)	ENSP00000352154.5:p.Glu23768=
ENST00000460472.6:c.70927G= (TTN)	ENSP00000434586.1:p.Glu23643=
ENST00000589042.5:c.98122G= (TTN) MANE Select	ENSP00000467141.1:p.Glu32708=
ENST00000591111.5:c.93199G= (TTN)	ENSP00000465570.1:p.Glu31067=
ENST00000615779.4:c.93199G= (TTN)	ENSP00000483597.1:p.Glu31067=
NM_001256850.1:c.93199G= (TTN)	NP_001243779.1:p.Glu31067=
NM_001267550.2:c.98122G= (TTN) MANE Select	NP_001254479.2:p.Glu32708=
NM_003319.4:c.70927G= (TTN)	NP_003310.4:p.Glu23643=
NM_133378.4:c.90418G= (TTN)	NP_596869.4:p.Glu30140=
NM_133432.3:c.71302G= (TTN)	NP_597676.3:p.Glu23768=
NM_133437.4:c.71503G= (TTN)	NP_597681.4:p.Glu23835=
NR_038271.1:n.446+16307C= (TTN-AS1)
NR_038272.1:n.1840+53C= (TTN-AS1)
XM_011511729.1:c.97219G= (TTN)	XP_011510031.1:p.Glu32407=
XM_011511730.1:c.71113G= (TTN)	XP_011510032.1:p.Glu23705=
XM_011511731.1:c.70972G= (TTN)	XP_011510033.1:p.Glu23658=
XM_017004819.1:c.97015G= (TTN)	XP_016860308.1:p.Glu32339=
XM_017004820.1:c.92413G= (TTN)	XP_016860309.1:p.Glu30805=
XM_017004821.1:c.92410G= (TTN)	XP_016860310.1:p.Glu30804=
XM_017004822.1:c.89452G= (TTN)	XP_016860311.1:p.Glu29818=
XM_017004823.1:c.71068G= (TTN)	XP_016860312.1:p.Glu23690=
XM_024453094.1:c.92563G= (TTN)	XP_024308862.1:p.Glu30855=
XM_024453095.1:c.92560G= (TTN)	XP_024308863.1:p.Glu30854=
XM_024453096.1:c.91993G= (TTN)	XP_024308864.1:p.Glu30665=
XM_024453097.1:c.89335G= (TTN)	XP_024308865.1:p.Glu29779=
XM_024453098.1:c.89254G= (TTN)	XP_024308866.1:p.Glu29752=
XM_024453099.1:c.71017G= (TTN)	XP_024308867.1:p.Glu23673=
XM_024453100.1:c.60871G= (TTN)	XP_024308868.1:p.Glu20291=