Canonical Allele Identifier: CA1310540933

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178594030C= , CM000664.2:g.178594030C=	GRCh38
NC_000002.11:g.179458757C= , CM000664.1:g.179458757C=	GRCh37
NC_000002.10:g.179167003C=	NCBI36
NG_011618.3:g.241773G= , LRG_391:g.241773G=
NG_051363.1:g.76204C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.50659G= (TTN)	ENSP00000343764.6:p.Gly16887=
ENST00000342175.11:c.31744G= (TTN)	ENSP00000340554.6:p.Gly10582=
ENST00000359218.10:c.31543G= (TTN)	ENSP00000352154.5:p.Gly10515=
ENST00000342175.10:c.31744G= (TTN)	ENSP00000340554.6:p.Gly10582=
ENST00000342992.10:c.50659G= (TTN)	ENSP00000343764.6:p.Gly16887=
ENST00000359218.9:c.31543G= (TTN)	ENSP00000352154.5:p.Gly10515=
ENST00000460472.6:c.31168G= (TTN)	ENSP00000434586.1:p.Gly10390=
ENST00000589042.5:c.58363G= (TTN) MANE Select	ENSP00000467141.1:p.Gly19455=
ENST00000591111.5:c.53440G= (TTN)	ENSP00000465570.1:p.Gly17814=
ENST00000615779.4:c.53440G= (TTN)	ENSP00000483597.1:p.Gly17814=
NM_001256850.1:c.53440G= (TTN)	NP_001243779.1:p.Gly17814=
NM_001267550.2:c.58363G= (TTN) MANE Select	NP_001254479.2:p.Gly19455=
NM_003319.4:c.31168G= (TTN)	NP_003310.4:p.Gly10390=
NM_133378.4:c.50659G= (TTN)	NP_596869.4:p.Gly16887=
NM_133432.3:c.31543G= (TTN)	NP_597676.3:p.Gly10515=
NM_133437.4:c.31744G= (TTN)	NP_597681.4:p.Gly10582=
NR_038271.1:n.597-3566C= (TTN-AS1)
NR_038272.1:n.3364+2716C= (TTN-AS1)
XM_011511729.1:c.57460G= (TTN)	XP_011510031.1:p.Gly19154=
XM_011511730.1:c.31354G= (TTN)	XP_011510032.1:p.Gly10452=
XM_011511731.1:c.31213G= (TTN)	XP_011510033.1:p.Gly10405=
XM_017004819.1:c.57256G= (TTN)	XP_016860308.1:p.Gly19086=
XM_017004820.1:c.52654G= (TTN)	XP_016860309.1:p.Gly17552=
XM_017004821.1:c.52651G= (TTN)	XP_016860310.1:p.Gly17551=
XM_017004822.1:c.49693G= (TTN)	XP_016860311.1:p.Gly16565=
XM_017004823.1:c.31309G= (TTN)	XP_016860312.1:p.Gly10437=
XM_024453094.1:c.52804G= (TTN)	XP_024308862.1:p.Gly17602=
XM_024453095.1:c.52801G= (TTN)	XP_024308863.1:p.Gly17601=
XM_024453096.1:c.52234G= (TTN)	XP_024308864.1:p.Gly17412=
XM_024453097.1:c.49576G= (TTN)	XP_024308865.1:p.Gly16526=
XM_024453098.1:c.49495G= (TTN)	XP_024308866.1:p.Gly16499=
XM_024453099.1:c.31258G= (TTN)	XP_024308867.1:p.Gly10420=
XM_024453100.1:c.21112G= (TTN)	XP_024308868.1:p.Gly7038=