Canonical Allele Identifier: CA1310530867

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178568994T= , CM000664.2:g.178568994T=	GRCh38
NC_000002.11:g.179433721T= , CM000664.1:g.179433721T=	GRCh37
NC_000002.10:g.179141967T=	NCBI36
NG_011618.3:g.266809A= , LRG_391:g.266809A=
NG_051363.1:g.51168T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.69434A= (TTN)	ENSP00000343764.6:p.Asn23145=
ENST00000342175.11:c.50519A= (TTN)	ENSP00000340554.6:p.Asn16840=
ENST00000359218.10:c.50318A= (TTN)	ENSP00000352154.5:p.Asn16773=
ENST00000342175.10:c.50519A= (TTN)	ENSP00000340554.6:p.Asn16840=
ENST00000342992.10:c.69434A= (TTN)	ENSP00000343764.6:p.Asn23145=
ENST00000359218.9:c.50318A= (TTN)	ENSP00000352154.5:p.Asn16773=
ENST00000460472.6:c.49943A= (TTN)	ENSP00000434586.1:p.Asn16648=
ENST00000589042.5:c.77138A= (TTN) MANE Select	ENSP00000467141.1:p.Asn25713=
ENST00000591111.5:c.72215A= (TTN)	ENSP00000465570.1:p.Asn24072=
ENST00000615779.4:c.72215A= (TTN)	ENSP00000483597.1:p.Asn24072=
NM_001256850.1:c.72215A= (TTN)	NP_001243779.1:p.Asn24072=
NM_001267550.2:c.77138A= (TTN) MANE Select	NP_001254479.2:p.Asn25713=
NM_003319.4:c.49943A= (TTN)	NP_003310.4:p.Asn16648=
NM_133378.4:c.69434A= (TTN)	NP_596869.4:p.Asn23145=
NM_133432.3:c.50318A= (TTN)	NP_597676.3:p.Asn16773=
NM_133437.4:c.50519A= (TTN)	NP_597681.4:p.Asn16840=
NR_038271.1:n.447-2306T= (TTN-AS1)
NR_038272.1:n.2044-13578T= (TTN-AS1)
XM_011511729.1:c.76235A= (TTN)	XP_011510031.1:p.Asn25412=
XM_011511730.1:c.50129A= (TTN)	XP_011510032.1:p.Asn16710=
XM_011511731.1:c.49988A= (TTN)	XP_011510033.1:p.Asn16663=
XM_017004819.1:c.76031A= (TTN)	XP_016860308.1:p.Asn25344=
XM_017004820.1:c.71429A= (TTN)	XP_016860309.1:p.Asn23810=
XM_017004821.1:c.71426A= (TTN)	XP_016860310.1:p.Asn23809=
XM_017004822.1:c.68468A= (TTN)	XP_016860311.1:p.Asn22823=
XM_017004823.1:c.50084A= (TTN)	XP_016860312.1:p.Asn16695=
XM_024453094.1:c.71579A= (TTN)	XP_024308862.1:p.Asn23860=
XM_024453095.1:c.71576A= (TTN)	XP_024308863.1:p.Asn23859=
XM_024453096.1:c.71009A= (TTN)	XP_024308864.1:p.Asn23670=
XM_024453097.1:c.68351A= (TTN)	XP_024308865.1:p.Asn22784=
XM_024453098.1:c.68270A= (TTN)	XP_024308866.1:p.Asn22757=
XM_024453099.1:c.50033A= (TTN)	XP_024308867.1:p.Asn16678=
XM_024453100.1:c.39887A= (TTN)	XP_024308868.1:p.Asn13296=