Canonical Allele Identifier: CA1310537207

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178584899C= , CM000664.2:g.178584899C=	GRCh38
NC_000002.11:g.179449626C= , CM000664.1:g.179449626C=	GRCh37
NC_000002.10:g.179157872C=	NCBI36
NG_011618.3:g.250904G= , LRG_391:g.250904G=
NG_051363.1:g.67073C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.64742G= (TTN) MANE Select	NP_001254479.2:p.Trp21581=
ENST00000589042.5:c.64742G= (TTN) MANE Select	ENSP00000467141.1:p.Trp21581=
NM_001256850.1:c.59819G= (TTN)	NP_001243779.1:p.Trp19940=
NM_003319.4:c.37547G= (TTN)	NP_003310.4:p.Trp12516=
NM_133378.4:c.57038G= (TTN)	NP_596869.4:p.Trp19013=
NM_133432.3:c.37922G= (TTN)	NP_597676.3:p.Trp12641=
NM_133437.4:c.38123G= (TTN)	NP_597681.4:p.Trp12708=
NR_038271.1:n.597-12697C= (TTN-AS1)
NR_038272.1:n.3094C= (TTN-AS1)
ENST00000342175.10:c.38123G= (TTN)	ENSP00000340554.6:p.Trp12708=
ENST00000342175.11:c.38123G= (TTN)	ENSP00000340554.6:p.Trp12708=
ENST00000342992.10:c.57038G= (TTN)	ENSP00000343764.6:p.Trp19013=
ENST00000342992.11:c.57038G= (TTN)	ENSP00000343764.6:p.Trp19013=
ENST00000359218.10:c.37922G= (TTN)	ENSP00000352154.5:p.Trp12641=
ENST00000359218.9:c.37922G= (TTN)	ENSP00000352154.5:p.Trp12641=
ENST00000460472.6:c.37547G= (TTN)	ENSP00000434586.1:p.Trp12516=
ENST00000591111.5:c.59819G= (TTN)	ENSP00000465570.1:p.Trp19940=
ENST00000615779.4:c.59819G= (TTN)	ENSP00000483597.1:p.Trp19940=
XM_011511729.1:c.63839G= (TTN)	XP_011510031.1:p.Trp21280=
XM_011511730.1:c.37733G= (TTN)	XP_011510032.1:p.Trp12578=
XM_011511731.1:c.37592G= (TTN)	XP_011510033.1:p.Trp12531=
XM_017004819.1:c.63635G= (TTN)	XP_016860308.1:p.Trp21212=
XM_017004820.1:c.59033G= (TTN)	XP_016860309.1:p.Trp19678=
XM_017004821.1:c.59030G= (TTN)	XP_016860310.1:p.Trp19677=
XM_017004822.1:c.56072G= (TTN)	XP_016860311.1:p.Trp18691=
XM_017004823.1:c.37688G= (TTN)	XP_016860312.1:p.Trp12563=
XM_024453094.1:c.59183G= (TTN)	XP_024308862.1:p.Trp19728=
XM_024453095.1:c.59180G= (TTN)	XP_024308863.1:p.Trp19727=
XM_024453096.1:c.58613G= (TTN)	XP_024308864.1:p.Trp19538=
XM_024453097.1:c.55955G= (TTN)	XP_024308865.1:p.Trp18652=
XM_024453098.1:c.55874G= (TTN)	XP_024308866.1:p.Trp18625=
XM_024453099.1:c.37637G= (TTN)	XP_024308867.1:p.Trp12546=
XM_024453100.1:c.27491G= (TTN)	XP_024308868.1:p.Trp9164=