Canonical Allele Identifier: CA1310521201

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543932A= , CM000664.2:g.178543932A=	GRCh38
NC_000002.11:g.179408659A= , CM000664.1:g.179408659A=	GRCh37
NC_000002.10:g.179116905A=	NCBI36
NG_011618.3:g.291871T= , LRG_391:g.291871T=
NG_051363.1:g.26106A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88508T= (TTN)	ENSP00000343764.6:p.Ile29503=
ENST00000342175.11:c.69593T= (TTN)	ENSP00000340554.6:p.Ile23198=
ENST00000359218.10:c.69392T= (TTN)	ENSP00000352154.5:p.Ile23131=
ENST00000342175.10:c.69593T= (TTN)	ENSP00000340554.6:p.Ile23198=
ENST00000342992.10:c.88508T= (TTN)	ENSP00000343764.6:p.Ile29503=
ENST00000359218.9:c.69392T= (TTN)	ENSP00000352154.5:p.Ile23131=
ENST00000460472.6:c.69017T= (TTN)	ENSP00000434586.1:p.Ile23006=
ENST00000589042.5:c.96212T= (TTN) MANE Select	ENSP00000467141.1:p.Ile32071=
ENST00000591111.5:c.91289T= (TTN)	ENSP00000465570.1:p.Ile30430=
ENST00000615779.4:c.91289T= (TTN)	ENSP00000483597.1:p.Ile30430=
NM_001256850.1:c.91289T= (TTN)	NP_001243779.1:p.Ile30430=
NM_001267550.2:c.96212T= (TTN) MANE Select	NP_001254479.2:p.Ile32071=
NM_003319.4:c.69017T= (TTN)	NP_003310.4:p.Ile23006=
NM_133378.4:c.88508T= (TTN)	NP_596869.4:p.Ile29503=
NM_133432.3:c.69392T= (TTN)	NP_597676.3:p.Ile23131=
NM_133437.4:c.69593T= (TTN)	NP_597681.4:p.Ile23198=
NR_038271.1:n.446+20296A= (TTN-AS1)
NR_038272.1:n.2043+1571A= (TTN-AS1)
XM_011511729.1:c.95309T= (TTN)	XP_011510031.1:p.Ile31770=
XM_011511730.1:c.69203T= (TTN)	XP_011510032.1:p.Ile23068=
XM_011511731.1:c.69062T= (TTN)	XP_011510033.1:p.Ile23021=
XM_017004819.1:c.95105T= (TTN)	XP_016860308.1:p.Ile31702=
XM_017004820.1:c.90503T= (TTN)	XP_016860309.1:p.Ile30168=
XM_017004821.1:c.90500T= (TTN)	XP_016860310.1:p.Ile30167=
XM_017004822.1:c.87542T= (TTN)	XP_016860311.1:p.Ile29181=
XM_017004823.1:c.69158T= (TTN)	XP_016860312.1:p.Ile23053=
XM_024453094.1:c.90653T= (TTN)	XP_024308862.1:p.Ile30218=
XM_024453095.1:c.90650T= (TTN)	XP_024308863.1:p.Ile30217=
XM_024453096.1:c.90083T= (TTN)	XP_024308864.1:p.Ile30028=
XM_024453097.1:c.87425T= (TTN)	XP_024308865.1:p.Ile29142=
XM_024453098.1:c.87344T= (TTN)	XP_024308866.1:p.Ile29115=
XM_024453099.1:c.69107T= (TTN)	XP_024308867.1:p.Ile23036=
XM_024453100.1:c.58961T= (TTN)	XP_024308868.1:p.Ile19654=