Canonical Allele Identifier: CA1310525928

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178557795C= , CM000664.2:g.178557795C=	GRCh38
NC_000002.11:g.179422522C= , CM000664.1:g.179422522C=	GRCh37
NC_000002.10:g.179130768C=	NCBI36
NG_011618.3:g.278008G= , LRG_391:g.278008G=
NG_051363.1:g.39969C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.79855G= (TTN)	ENSP00000343764.6:p.Glu26619=
ENST00000342175.11:c.60940G= (TTN)	ENSP00000340554.6:p.Glu20314=
ENST00000359218.10:c.60739G= (TTN)	ENSP00000352154.5:p.Glu20247=
ENST00000342175.10:c.60940G= (TTN)	ENSP00000340554.6:p.Glu20314=
ENST00000342992.10:c.79855G= (TTN)	ENSP00000343764.6:p.Glu26619=
ENST00000359218.9:c.60739G= (TTN)	ENSP00000352154.5:p.Glu20247=
ENST00000460472.6:c.60364G= (TTN)	ENSP00000434586.1:p.Glu20122=
ENST00000589042.5:c.87559G= (TTN) MANE Select	ENSP00000467141.1:p.Glu29187=
ENST00000591111.5:c.82636G= (TTN)	ENSP00000465570.1:p.Glu27546=
ENST00000615779.4:c.82636G= (TTN)	ENSP00000483597.1:p.Glu27546=
NM_001256850.1:c.82636G= (TTN)	NP_001243779.1:p.Glu27546=
NM_001267550.2:c.87559G= (TTN) MANE Select	NP_001254479.2:p.Glu29187=
NM_003319.4:c.60364G= (TTN)	NP_003310.4:p.Glu20122=
NM_133378.4:c.79855G= (TTN)	NP_596869.4:p.Glu26619=
NM_133432.3:c.60739G= (TTN)	NP_597676.3:p.Glu20247=
NM_133437.4:c.60940G= (TTN)	NP_597681.4:p.Glu20314=
NR_038271.1:n.447-13505C= (TTN-AS1)
NR_038272.1:n.2043+15434C= (TTN-AS1)
XM_011511729.1:c.86656G= (TTN)	XP_011510031.1:p.Glu28886=
XM_011511730.1:c.60550G= (TTN)	XP_011510032.1:p.Glu20184=
XM_011511731.1:c.60409G= (TTN)	XP_011510033.1:p.Glu20137=
XM_017004819.1:c.86452G= (TTN)	XP_016860308.1:p.Glu28818=
XM_017004820.1:c.81850G= (TTN)	XP_016860309.1:p.Glu27284=
XM_017004821.1:c.81847G= (TTN)	XP_016860310.1:p.Glu27283=
XM_017004822.1:c.78889G= (TTN)	XP_016860311.1:p.Glu26297=
XM_017004823.1:c.60505G= (TTN)	XP_016860312.1:p.Glu20169=
XM_024453094.1:c.82000G= (TTN)	XP_024308862.1:p.Glu27334=
XM_024453095.1:c.81997G= (TTN)	XP_024308863.1:p.Glu27333=
XM_024453096.1:c.81430G= (TTN)	XP_024308864.1:p.Glu27144=
XM_024453097.1:c.78772G= (TTN)	XP_024308865.1:p.Glu26258=
XM_024453098.1:c.78691G= (TTN)	XP_024308866.1:p.Glu26231=
XM_024453099.1:c.60454G= (TTN)	XP_024308867.1:p.Glu20152=
XM_024453100.1:c.50308G= (TTN)	XP_024308868.1:p.Glu16770=