Canonical Allele Identifier: CA1310523383

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178546765G= , CM000664.2:g.178546765G=	GRCh38
NC_000002.11:g.179411492G= , CM000664.1:g.179411492G=	GRCh37
NC_000002.10:g.179119738G=	NCBI36
NG_011618.3:g.289038C= , LRG_391:g.289038C=
NG_051363.1:g.28939G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.86959C= (TTN)	ENSP00000343764.6:p.Arg28987=
ENST00000342175.11:c.68044C= (TTN)	ENSP00000340554.6:p.Arg22682=
ENST00000359218.10:c.67843C= (TTN)	ENSP00000352154.5:p.Arg22615=
ENST00000342175.10:c.68044C= (TTN)	ENSP00000340554.6:p.Arg22682=
ENST00000342992.10:c.86959C= (TTN)	ENSP00000343764.6:p.Arg28987=
ENST00000359218.9:c.67843C= (TTN)	ENSP00000352154.5:p.Arg22615=
ENST00000460472.6:c.67468C= (TTN)	ENSP00000434586.1:p.Arg22490=
ENST00000589042.5:c.94663C= (TTN) MANE Select	ENSP00000467141.1:p.Arg31555=
ENST00000591111.5:c.89740C= (TTN)	ENSP00000465570.1:p.Arg29914=
ENST00000615779.4:c.89740C= (TTN)	ENSP00000483597.1:p.Arg29914=
NM_001256850.1:c.89740C= (TTN)	NP_001243779.1:p.Arg29914=
NM_001267550.2:c.94663C= (TTN) MANE Select	NP_001254479.2:p.Arg31555=
NM_003319.4:c.67468C= (TTN)	NP_003310.4:p.Arg22490=
NM_133378.4:c.86959C= (TTN)	NP_596869.4:p.Arg28987=
NM_133432.3:c.67843C= (TTN)	NP_597676.3:p.Arg22615=
NM_133437.4:c.68044C= (TTN)	NP_597681.4:p.Arg22682=
NR_038271.1:n.446+23129G= (TTN-AS1)
NR_038272.1:n.2043+4404G= (TTN-AS1)
XM_011511729.1:c.93760C= (TTN)	XP_011510031.1:p.Arg31254=
XM_011511730.1:c.67654C= (TTN)	XP_011510032.1:p.Arg22552=
XM_011511731.1:c.67513C= (TTN)	XP_011510033.1:p.Arg22505=
XM_017004819.1:c.93556C= (TTN)	XP_016860308.1:p.Arg31186=
XM_017004820.1:c.88954C= (TTN)	XP_016860309.1:p.Arg29652=
XM_017004821.1:c.88951C= (TTN)	XP_016860310.1:p.Arg29651=
XM_017004822.1:c.85993C= (TTN)	XP_016860311.1:p.Arg28665=
XM_017004823.1:c.67609C= (TTN)	XP_016860312.1:p.Arg22537=
XM_024453094.1:c.89104C= (TTN)	XP_024308862.1:p.Arg29702=
XM_024453095.1:c.89101C= (TTN)	XP_024308863.1:p.Arg29701=
XM_024453096.1:c.88534C= (TTN)	XP_024308864.1:p.Arg29512=
XM_024453097.1:c.85876C= (TTN)	XP_024308865.1:p.Arg28626=
XM_024453098.1:c.85795C= (TTN)	XP_024308866.1:p.Arg28599=
XM_024453099.1:c.67558C= (TTN)	XP_024308867.1:p.Arg22520=
XM_024453100.1:c.57412C= (TTN)	XP_024308868.1:p.Arg19138=