Canonical Allele Identifier: CA1310525934

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178557806G= , CM000664.2:g.178557806G=	GRCh38
NC_000002.11:g.179422533G= , CM000664.1:g.179422533G=	GRCh37
NC_000002.10:g.179130779G=	NCBI36
NG_011618.3:g.277997C= , LRG_391:g.277997C=
NG_051363.1:g.39980G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.79844C= (TTN)	ENSP00000343764.6:p.Ala26615=
ENST00000342175.11:c.60929C= (TTN)	ENSP00000340554.6:p.Ala20310=
ENST00000359218.10:c.60728C= (TTN)	ENSP00000352154.5:p.Ala20243=
ENST00000342175.10:c.60929C= (TTN)	ENSP00000340554.6:p.Ala20310=
ENST00000342992.10:c.79844C= (TTN)	ENSP00000343764.6:p.Ala26615=
ENST00000359218.9:c.60728C= (TTN)	ENSP00000352154.5:p.Ala20243=
ENST00000460472.6:c.60353C= (TTN)	ENSP00000434586.1:p.Ala20118=
ENST00000589042.5:c.87548C= (TTN) MANE Select	ENSP00000467141.1:p.Ala29183=
ENST00000591111.5:c.82625C= (TTN)	ENSP00000465570.1:p.Ala27542=
ENST00000615779.4:c.82625C= (TTN)	ENSP00000483597.1:p.Ala27542=
NM_001256850.1:c.82625C= (TTN)	NP_001243779.1:p.Ala27542=
NM_001267550.2:c.87548C= (TTN) MANE Select	NP_001254479.2:p.Ala29183=
NM_003319.4:c.60353C= (TTN)	NP_003310.4:p.Ala20118=
NM_133378.4:c.79844C= (TTN)	NP_596869.4:p.Ala26615=
NM_133432.3:c.60728C= (TTN)	NP_597676.3:p.Ala20243=
NM_133437.4:c.60929C= (TTN)	NP_597681.4:p.Ala20310=
NR_038271.1:n.447-13494G= (TTN-AS1)
NR_038272.1:n.2043+15445G= (TTN-AS1)
XM_011511729.1:c.86645C= (TTN)	XP_011510031.1:p.Ala28882=
XM_011511730.1:c.60539C= (TTN)	XP_011510032.1:p.Ala20180=
XM_011511731.1:c.60398C= (TTN)	XP_011510033.1:p.Ala20133=
XM_017004819.1:c.86441C= (TTN)	XP_016860308.1:p.Ala28814=
XM_017004820.1:c.81839C= (TTN)	XP_016860309.1:p.Ala27280=
XM_017004821.1:c.81836C= (TTN)	XP_016860310.1:p.Ala27279=
XM_017004822.1:c.78878C= (TTN)	XP_016860311.1:p.Ala26293=
XM_017004823.1:c.60494C= (TTN)	XP_016860312.1:p.Ala20165=
XM_024453094.1:c.81989C= (TTN)	XP_024308862.1:p.Ala27330=
XM_024453095.1:c.81986C= (TTN)	XP_024308863.1:p.Ala27329=
XM_024453096.1:c.81419C= (TTN)	XP_024308864.1:p.Ala27140=
XM_024453097.1:c.78761C= (TTN)	XP_024308865.1:p.Ala26254=
XM_024453098.1:c.78680C= (TTN)	XP_024308866.1:p.Ala26227=
XM_024453099.1:c.60443C= (TTN)	XP_024308867.1:p.Ala20148=
XM_024453100.1:c.50297C= (TTN)	XP_024308868.1:p.Ala16766=