Canonical Allele Identifier: CA1310514609

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530413T= , CM000664.2:g.178530413T=	GRCh38
NC_000002.11:g.179395140T= , CM000664.1:g.179395140T=	GRCh37
NC_000002.10:g.179103386T=	NCBI36
NG_011618.3:g.305390A= , LRG_391:g.305390A=
NG_051363.1:g.12587T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98498A= (TTN)	ENSP00000343764.6:p.Glu32833=
ENST00000342175.11:c.79583A= (TTN)	ENSP00000340554.6:p.Glu26528=
ENST00000359218.10:c.79382A= (TTN)	ENSP00000352154.5:p.Glu26461=
ENST00000342175.10:c.79583A= (TTN)	ENSP00000340554.6:p.Glu26528=
ENST00000342992.10:c.98498A= (TTN)	ENSP00000343764.6:p.Glu32833=
ENST00000359218.9:c.79382A= (TTN)	ENSP00000352154.5:p.Glu26461=
ENST00000460472.6:c.79007A= (TTN)	ENSP00000434586.1:p.Glu26336=
ENST00000589042.5:c.106202A= (TTN) MANE Select	ENSP00000467141.1:p.Glu35401=
ENST00000591111.5:c.101279A= (TTN)	ENSP00000465570.1:p.Glu33760=
ENST00000615779.4:c.101279A= (TTN)	ENSP00000483597.1:p.Glu33760=
NM_001256850.1:c.101279A= (TTN)	NP_001243779.1:p.Glu33760=
NM_001267550.2:c.106202A= (TTN) MANE Select	NP_001254479.2:p.Glu35401=
NM_003319.4:c.79007A= (TTN)	NP_003310.4:p.Glu26336=
NM_133378.4:c.98498A= (TTN)	NP_596869.4:p.Glu32833=
NM_133432.3:c.79382A= (TTN)	NP_597676.3:p.Glu26461=
NM_133437.4:c.79583A= (TTN)	NP_597681.4:p.Glu26528=
NR_038271.1:n.446+6777T= (TTN-AS1)
NR_038272.1:n.220-5319T= (TTN-AS1)
XM_011511729.1:c.105299A= (TTN)	XP_011510031.1:p.Glu35100=
XM_011511730.1:c.79193A= (TTN)	XP_011510032.1:p.Glu26398=
XM_011511731.1:c.79052A= (TTN)	XP_011510033.1:p.Glu26351=
XM_017004819.1:c.105095A= (TTN)	XP_016860308.1:p.Glu35032=
XM_017004820.1:c.100493A= (TTN)	XP_016860309.1:p.Glu33498=
XM_017004821.1:c.100490A= (TTN)	XP_016860310.1:p.Glu33497=
XM_017004822.1:c.97532A= (TTN)	XP_016860311.1:p.Glu32511=
XM_017004823.1:c.79148A= (TTN)	XP_016860312.1:p.Glu26383=
XM_024453094.1:c.100643A= (TTN)	XP_024308862.1:p.Glu33548=
XM_024453095.1:c.100640A= (TTN)	XP_024308863.1:p.Glu33547=
XM_024453096.1:c.100073A= (TTN)	XP_024308864.1:p.Glu33358=
XM_024453097.1:c.97415A= (TTN)	XP_024308865.1:p.Glu32472=
XM_024453098.1:c.97334A= (TTN)	XP_024308866.1:p.Glu32445=
XM_024453099.1:c.79097A= (TTN)	XP_024308867.1:p.Glu26366=
XM_024453100.1:c.68951A= (TTN)	XP_024308868.1:p.Glu22984=