Canonical Allele Identifier: CA1310511396

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530053G= , CM000664.2:g.178530053G=	GRCh38
NC_000002.11:g.179394780G= , CM000664.1:g.179394780G=	GRCh37
NC_000002.10:g.179103026G=	NCBI36
NG_011618.3:g.305750C= , LRG_391:g.305750C=
NG_051363.1:g.12227G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98734C= (TTN)	ENSP00000343764.6:p.His32912=
ENST00000342175.11:c.79819C= (TTN)	ENSP00000340554.6:p.His26607=
ENST00000359218.10:c.79618C= (TTN)	ENSP00000352154.5:p.His26540=
ENST00000342175.10:c.79819C= (TTN)	ENSP00000340554.6:p.His26607=
ENST00000342992.10:c.98734C= (TTN)	ENSP00000343764.6:p.His32912=
ENST00000359218.9:c.79618C= (TTN)	ENSP00000352154.5:p.His26540=
ENST00000460472.6:c.79243C= (TTN)	ENSP00000434586.1:p.His26415=
ENST00000589042.5:c.106438C= (TTN) MANE Select	ENSP00000467141.1:p.His35480=
ENST00000591111.5:c.101515C= (TTN)	ENSP00000465570.1:p.His33839=
ENST00000615779.4:c.101515C= (TTN)	ENSP00000483597.1:p.His33839=
NM_001256850.1:c.101515C= (TTN)	NP_001243779.1:p.His33839=
NM_001267550.2:c.106438C= (TTN) MANE Select	NP_001254479.2:p.His35480=
NM_003319.4:c.79243C= (TTN)	NP_003310.4:p.His26415=
NM_133378.4:c.98734C= (TTN)	NP_596869.4:p.His32912=
NM_133432.3:c.79618C= (TTN)	NP_597676.3:p.His26540=
NM_133437.4:c.79819C= (TTN)	NP_597681.4:p.His26607=
NR_038271.1:n.446+6417G= (TTN-AS1)
NR_038272.1:n.220-5679G= (TTN-AS1)
XM_011511729.1:c.105535C= (TTN)	XP_011510031.1:p.His35179=
XM_011511730.1:c.79429C= (TTN)	XP_011510032.1:p.His26477=
XM_011511731.1:c.79288C= (TTN)	XP_011510033.1:p.His26430=
XM_017004819.1:c.105331C= (TTN)	XP_016860308.1:p.His35111=
XM_017004820.1:c.100729C= (TTN)	XP_016860309.1:p.His33577=
XM_017004821.1:c.100726C= (TTN)	XP_016860310.1:p.His33576=
XM_017004822.1:c.97768C= (TTN)	XP_016860311.1:p.His32590=
XM_017004823.1:c.79384C= (TTN)	XP_016860312.1:p.His26462=
XM_024453094.1:c.100879C= (TTN)	XP_024308862.1:p.His33627=
XM_024453095.1:c.100876C= (TTN)	XP_024308863.1:p.His33626=
XM_024453096.1:c.100309C= (TTN)	XP_024308864.1:p.His33437=
XM_024453097.1:c.97651C= (TTN)	XP_024308865.1:p.His32551=
XM_024453098.1:c.97570C= (TTN)	XP_024308866.1:p.His32524=
XM_024453099.1:c.79333C= (TTN)	XP_024308867.1:p.His26445=
XM_024453100.1:c.69187C= (TTN)	XP_024308868.1:p.His23063=