Canonical Allele Identifier: CA1310521327

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544093T= , CM000664.2:g.178544093T=	GRCh38
NC_000002.11:g.179408820T= , CM000664.1:g.179408820T=	GRCh37
NC_000002.10:g.179117066T=	NCBI36
NG_011618.3:g.291710A= , LRG_391:g.291710A=
NG_051363.1:g.26267T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88347A= (TTN)	ENSP00000343764.6:p.Ala29449=
ENST00000342175.11:c.69432A= (TTN)	ENSP00000340554.6:p.Ala23144=
ENST00000359218.10:c.69231A= (TTN)	ENSP00000352154.5:p.Ala23077=
ENST00000342175.10:c.69432A= (TTN)	ENSP00000340554.6:p.Ala23144=
ENST00000342992.10:c.88347A= (TTN)	ENSP00000343764.6:p.Ala29449=
ENST00000359218.9:c.69231A= (TTN)	ENSP00000352154.5:p.Ala23077=
ENST00000460472.6:c.68856A= (TTN)	ENSP00000434586.1:p.Ala22952=
ENST00000589042.5:c.96051A= (TTN) MANE Select	ENSP00000467141.1:p.Ala32017=
ENST00000591111.5:c.91128A= (TTN)	ENSP00000465570.1:p.Ala30376=
ENST00000615779.4:c.91128A= (TTN)	ENSP00000483597.1:p.Ala30376=
NM_001256850.1:c.91128A= (TTN)	NP_001243779.1:p.Ala30376=
NM_001267550.2:c.96051A= (TTN) MANE Select	NP_001254479.2:p.Ala32017=
NM_003319.4:c.68856A= (TTN)	NP_003310.4:p.Ala22952=
NM_133378.4:c.88347A= (TTN)	NP_596869.4:p.Ala29449=
NM_133432.3:c.69231A= (TTN)	NP_597676.3:p.Ala23077=
NM_133437.4:c.69432A= (TTN)	NP_597681.4:p.Ala23144=
NR_038271.1:n.446+20457T= (TTN-AS1)
NR_038272.1:n.2043+1732T= (TTN-AS1)
XM_011511729.1:c.95148A= (TTN)	XP_011510031.1:p.Ala31716=
XM_011511730.1:c.69042A= (TTN)	XP_011510032.1:p.Ala23014=
XM_011511731.1:c.68901A= (TTN)	XP_011510033.1:p.Ala22967=
XM_017004819.1:c.94944A= (TTN)	XP_016860308.1:p.Ala31648=
XM_017004820.1:c.90342A= (TTN)	XP_016860309.1:p.Ala30114=
XM_017004821.1:c.90339A= (TTN)	XP_016860310.1:p.Ala30113=
XM_017004822.1:c.87381A= (TTN)	XP_016860311.1:p.Ala29127=
XM_017004823.1:c.68997A= (TTN)	XP_016860312.1:p.Ala22999=
XM_024453094.1:c.90492A= (TTN)	XP_024308862.1:p.Ala30164=
XM_024453095.1:c.90489A= (TTN)	XP_024308863.1:p.Ala30163=
XM_024453096.1:c.89922A= (TTN)	XP_024308864.1:p.Ala29974=
XM_024453097.1:c.87264A= (TTN)	XP_024308865.1:p.Ala29088=
XM_024453098.1:c.87183A= (TTN)	XP_024308866.1:p.Ala29061=
XM_024453099.1:c.68946A= (TTN)	XP_024308867.1:p.Ala22982=
XM_024453100.1:c.58800A= (TTN)	XP_024308868.1:p.Ala19600=