Canonical Allele Identifier: CA1310550885

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618036C= , CM000664.2:g.178618036C=	GRCh38
NC_000002.11:g.179482763C= , CM000664.1:g.179482763C=	GRCh37
NC_000002.10:g.179191008C=	NCBI36
NG_011618.3:g.217767G= , LRG_391:g.217767G=
NG_051363.1:g.100210C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.39611G= (TTN)	ENSP00000343764.6:p.Arg13204=
ENST00000342175.11:c.20696G= (TTN)	ENSP00000340554.6:p.Arg6899=
ENST00000359218.10:c.20495G= (TTN)	ENSP00000352154.5:p.Arg6832=
ENST00000342175.10:c.20696G= (TTN)	ENSP00000340554.6:p.Arg6899=
ENST00000342992.10:c.39611G= (TTN)	ENSP00000343764.6:p.Arg13204=
ENST00000359218.9:c.20495G= (TTN)	ENSP00000352154.5:p.Arg6832=
ENST00000460472.6:c.20120G= (TTN)	ENSP00000434586.1:p.Arg6707=
ENST00000589042.5:c.47315G= (TTN) MANE Select	ENSP00000467141.1:p.Arg15772=
ENST00000591111.5:c.42392G= (TTN)	ENSP00000465570.1:p.Arg14131=
ENST00000615779.4:c.42392G= (TTN)	ENSP00000483597.1:p.Arg14131=
NM_001256850.1:c.42392G= (TTN)	NP_001243779.1:p.Arg14131=
NM_001267550.2:c.47315G= (TTN) MANE Select	NP_001254479.2:p.Arg15772=
NM_003319.4:c.20120G= (TTN)	NP_003310.4:p.Arg6707=
NM_133378.4:c.39611G= (TTN)	NP_596869.4:p.Arg13204=
NM_133432.3:c.20495G= (TTN)	NP_597676.3:p.Arg6832=
NM_133437.4:c.20696G= (TTN)	NP_597681.4:p.Arg6899=
NR_038271.1:n.1605-1717C= (TTN-AS1)
XM_011511729.1:c.46412G= (TTN)	XP_011510031.1:p.Arg15471=
XM_011511730.1:c.20306G= (TTN)	XP_011510032.1:p.Arg6769=
XM_011511731.1:c.20165G= (TTN)	XP_011510033.1:p.Arg6722=
XM_017004819.1:c.46208G= (TTN)	XP_016860308.1:p.Arg15403=
XM_017004820.1:c.41606G= (TTN)	XP_016860309.1:p.Arg13869=
XM_017004821.1:c.41603G= (TTN)	XP_016860310.1:p.Arg13868=
XM_017004822.1:c.38645G= (TTN)	XP_016860311.1:p.Arg12882=
XM_017004823.1:c.20261G= (TTN)	XP_016860312.1:p.Arg6754=
XM_024453094.1:c.41756G= (TTN)	XP_024308862.1:p.Arg13919=
XM_024453095.1:c.41753G= (TTN)	XP_024308863.1:p.Arg13918=
XM_024453096.1:c.41186G= (TTN)	XP_024308864.1:p.Arg13729=
XM_024453097.1:c.38528G= (TTN)	XP_024308865.1:p.Arg12843=
XM_024453098.1:c.38447G= (TTN)	XP_024308866.1:p.Arg12816=
XM_024453099.1:c.20210G= (TTN)	XP_024308867.1:p.Arg6737=
XM_024453100.1:c.10064G= (TTN)	XP_024308868.1:p.Arg3355=