Canonical Allele Identifier: CA1310511423

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530069C= , CM000664.2:g.178530069C=	GRCh38
NC_000002.11:g.179394796C= , CM000664.1:g.179394796C=	GRCh37
NC_000002.10:g.179103042C=	NCBI36
NG_011618.3:g.305734G= , LRG_391:g.305734G=
NG_051363.1:g.12243C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98718G= (TTN)	ENSP00000343764.6:p.Gly32906=
ENST00000342175.11:c.79803G= (TTN)	ENSP00000340554.6:p.Gly26601=
ENST00000359218.10:c.79602G= (TTN)	ENSP00000352154.5:p.Gly26534=
ENST00000342175.10:c.79803G= (TTN)	ENSP00000340554.6:p.Gly26601=
ENST00000342992.10:c.98718G= (TTN)	ENSP00000343764.6:p.Gly32906=
ENST00000359218.9:c.79602G= (TTN)	ENSP00000352154.5:p.Gly26534=
ENST00000460472.6:c.79227G= (TTN)	ENSP00000434586.1:p.Gly26409=
ENST00000589042.5:c.106422G= (TTN) MANE Select	ENSP00000467141.1:p.Gly35474=
ENST00000591111.5:c.101499G= (TTN)	ENSP00000465570.1:p.Gly33833=
ENST00000615779.4:c.101499G= (TTN)	ENSP00000483597.1:p.Gly33833=
NM_001256850.1:c.101499G= (TTN)	NP_001243779.1:p.Gly33833=
NM_001267550.2:c.106422G= (TTN) MANE Select	NP_001254479.2:p.Gly35474=
NM_003319.4:c.79227G= (TTN)	NP_003310.4:p.Gly26409=
NM_133378.4:c.98718G= (TTN)	NP_596869.4:p.Gly32906=
NM_133432.3:c.79602G= (TTN)	NP_597676.3:p.Gly26534=
NM_133437.4:c.79803G= (TTN)	NP_597681.4:p.Gly26601=
NR_038271.1:n.446+6433C= (TTN-AS1)
NR_038272.1:n.220-5663C= (TTN-AS1)
XM_011511729.1:c.105519G= (TTN)	XP_011510031.1:p.Gly35173=
XM_011511730.1:c.79413G= (TTN)	XP_011510032.1:p.Gly26471=
XM_011511731.1:c.79272G= (TTN)	XP_011510033.1:p.Gly26424=
XM_017004819.1:c.105315G= (TTN)	XP_016860308.1:p.Gly35105=
XM_017004820.1:c.100713G= (TTN)	XP_016860309.1:p.Gly33571=
XM_017004821.1:c.100710G= (TTN)	XP_016860310.1:p.Gly33570=
XM_017004822.1:c.97752G= (TTN)	XP_016860311.1:p.Gly32584=
XM_017004823.1:c.79368G= (TTN)	XP_016860312.1:p.Gly26456=
XM_024453094.1:c.100863G= (TTN)	XP_024308862.1:p.Gly33621=
XM_024453095.1:c.100860G= (TTN)	XP_024308863.1:p.Gly33620=
XM_024453096.1:c.100293G= (TTN)	XP_024308864.1:p.Gly33431=
XM_024453097.1:c.97635G= (TTN)	XP_024308865.1:p.Gly32545=
XM_024453098.1:c.97554G= (TTN)	XP_024308866.1:p.Gly32518=
XM_024453099.1:c.79317G= (TTN)	XP_024308867.1:p.Gly26439=
XM_024453100.1:c.69171G= (TTN)	XP_024308868.1:p.Gly23057=