Canonical Allele Identifier: CA1310520136

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178549846G= , CM000664.2:g.178549846G=	GRCh38
NC_000002.11:g.179414573G= , CM000664.1:g.179414573G=	GRCh37
NC_000002.10:g.179122819G=	NCBI36
NG_011618.3:g.285957C= , LRG_391:g.285957C=
NG_051363.1:g.32020G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.84172C= (TTN)	ENSP00000343764.6:p.Pro28058=
ENST00000342175.11:c.65257C= (TTN)	ENSP00000340554.6:p.Pro21753=
ENST00000359218.10:c.65056C= (TTN)	ENSP00000352154.5:p.Pro21686=
ENST00000342175.10:c.65257C= (TTN)	ENSP00000340554.6:p.Pro21753=
ENST00000342992.10:c.84172C= (TTN)	ENSP00000343764.6:p.Pro28058=
ENST00000359218.9:c.65056C= (TTN)	ENSP00000352154.5:p.Pro21686=
ENST00000460472.6:c.64681C= (TTN)	ENSP00000434586.1:p.Pro21561=
ENST00000589042.5:c.91876C= (TTN) MANE Select	ENSP00000467141.1:p.Pro30626=
ENST00000591111.5:c.86953C= (TTN)	ENSP00000465570.1:p.Pro28985=
ENST00000615779.4:c.86953C= (TTN)	ENSP00000483597.1:p.Pro28985=
NM_001256850.1:c.86953C= (TTN)	NP_001243779.1:p.Pro28985=
NM_001267550.2:c.91876C= (TTN) MANE Select	NP_001254479.2:p.Pro30626=
NM_003319.4:c.64681C= (TTN)	NP_003310.4:p.Pro21561=
NM_133378.4:c.84172C= (TTN)	NP_596869.4:p.Pro28058=
NM_133432.3:c.65056C= (TTN)	NP_597676.3:p.Pro21686=
NM_133437.4:c.65257C= (TTN)	NP_597681.4:p.Pro21753=
NR_038271.1:n.447-21454G= (TTN-AS1)
NR_038272.1:n.2043+7485G= (TTN-AS1)
XM_011511729.1:c.90973C= (TTN)	XP_011510031.1:p.Pro30325=
XM_011511730.1:c.64867C= (TTN)	XP_011510032.1:p.Pro21623=
XM_011511731.1:c.64726C= (TTN)	XP_011510033.1:p.Pro21576=
XM_017004819.1:c.90769C= (TTN)	XP_016860308.1:p.Pro30257=
XM_017004820.1:c.86167C= (TTN)	XP_016860309.1:p.Pro28723=
XM_017004821.1:c.86164C= (TTN)	XP_016860310.1:p.Pro28722=
XM_017004822.1:c.83206C= (TTN)	XP_016860311.1:p.Pro27736=
XM_017004823.1:c.64822C= (TTN)	XP_016860312.1:p.Pro21608=
XM_024453094.1:c.86317C= (TTN)	XP_024308862.1:p.Pro28773=
XM_024453095.1:c.86314C= (TTN)	XP_024308863.1:p.Pro28772=
XM_024453096.1:c.85747C= (TTN)	XP_024308864.1:p.Pro28583=
XM_024453097.1:c.83089C= (TTN)	XP_024308865.1:p.Pro27697=
XM_024453098.1:c.83008C= (TTN)	XP_024308866.1:p.Pro27670=
XM_024453099.1:c.64771C= (TTN)	XP_024308867.1:p.Pro21591=
XM_024453100.1:c.54625C= (TTN)	XP_024308868.1:p.Pro18209=