Canonical Allele Identifier: CA1310514829

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530648C= , CM000664.2:g.178530648C=	GRCh38
NC_000002.11:g.179395375C= , CM000664.1:g.179395375C=	GRCh37
NC_000002.10:g.179103621C=	NCBI36
NG_011618.3:g.305155G= , LRG_391:g.305155G=
NG_051363.1:g.12822C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98263G= (TTN)	ENSP00000343764.6:p.Gly32755=
ENST00000342175.11:c.79348G= (TTN)	ENSP00000340554.6:p.Gly26450=
ENST00000359218.10:c.79147G= (TTN)	ENSP00000352154.5:p.Gly26383=
ENST00000342175.10:c.79348G= (TTN)	ENSP00000340554.6:p.Gly26450=
ENST00000342992.10:c.98263G= (TTN)	ENSP00000343764.6:p.Gly32755=
ENST00000359218.9:c.79147G= (TTN)	ENSP00000352154.5:p.Gly26383=
ENST00000460472.6:c.78772G= (TTN)	ENSP00000434586.1:p.Gly26258=
ENST00000589042.5:c.105967G= (TTN) MANE Select	ENSP00000467141.1:p.Gly35323=
ENST00000591111.5:c.101044G= (TTN)	ENSP00000465570.1:p.Gly33682=
ENST00000615779.4:c.101044G= (TTN)	ENSP00000483597.1:p.Gly33682=
NM_001256850.1:c.101044G= (TTN)	NP_001243779.1:p.Gly33682=
NM_001267550.2:c.105967G= (TTN) MANE Select	NP_001254479.2:p.Gly35323=
NM_003319.4:c.78772G= (TTN)	NP_003310.4:p.Gly26258=
NM_133378.4:c.98263G= (TTN)	NP_596869.4:p.Gly32755=
NM_133432.3:c.79147G= (TTN)	NP_597676.3:p.Gly26383=
NM_133437.4:c.79348G= (TTN)	NP_597681.4:p.Gly26450=
NR_038271.1:n.446+7012C= (TTN-AS1)
NR_038272.1:n.220-5084C= (TTN-AS1)
XM_011511729.1:c.105064G= (TTN)	XP_011510031.1:p.Gly35022=
XM_011511730.1:c.78958G= (TTN)	XP_011510032.1:p.Gly26320=
XM_011511731.1:c.78817G= (TTN)	XP_011510033.1:p.Gly26273=
XM_017004819.1:c.104860G= (TTN)	XP_016860308.1:p.Gly34954=
XM_017004820.1:c.100258G= (TTN)	XP_016860309.1:p.Gly33420=
XM_017004821.1:c.100255G= (TTN)	XP_016860310.1:p.Gly33419=
XM_017004822.1:c.97297G= (TTN)	XP_016860311.1:p.Gly32433=
XM_017004823.1:c.78913G= (TTN)	XP_016860312.1:p.Gly26305=
XM_024453094.1:c.100408G= (TTN)	XP_024308862.1:p.Gly33470=
XM_024453095.1:c.100405G= (TTN)	XP_024308863.1:p.Gly33469=
XM_024453096.1:c.99838G= (TTN)	XP_024308864.1:p.Gly33280=
XM_024453097.1:c.97180G= (TTN)	XP_024308865.1:p.Gly32394=
XM_024453098.1:c.97099G= (TTN)	XP_024308866.1:p.Gly32367=
XM_024453099.1:c.78862G= (TTN)	XP_024308867.1:p.Gly26288=
XM_024453100.1:c.68716G= (TTN)	XP_024308868.1:p.Gly22906=