Canonical Allele Identifier: CA1310546667

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178607680G= , CM000664.2:g.178607680G=	GRCh38
NC_000002.11:g.179472407G= , CM000664.1:g.179472407G=	GRCh37
NC_000002.10:g.179180652G=	NCBI36
NG_011618.3:g.228123C= , LRG_391:g.228123C=
NG_051363.1:g.89854G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.45304C= (TTN)	ENSP00000343764.6:p.Pro15102=
ENST00000342175.11:c.26389C= (TTN)	ENSP00000340554.6:p.Pro8797=
ENST00000359218.10:c.26188C= (TTN)	ENSP00000352154.5:p.Pro8730=
ENST00000342175.10:c.26389C= (TTN)	ENSP00000340554.6:p.Pro8797=
ENST00000342992.10:c.45304C= (TTN)	ENSP00000343764.6:p.Pro15102=
ENST00000359218.9:c.26188C= (TTN)	ENSP00000352154.5:p.Pro8730=
ENST00000460472.6:c.25813C= (TTN)	ENSP00000434586.1:p.Pro8605=
ENST00000589042.5:c.53008C= (TTN) MANE Select	ENSP00000467141.1:p.Pro17670=
ENST00000591111.5:c.48085C= (TTN)	ENSP00000465570.1:p.Pro16029=
ENST00000615779.4:c.48085C= (TTN)	ENSP00000483597.1:p.Pro16029=
NM_001256850.1:c.48085C= (TTN)	NP_001243779.1:p.Pro16029=
NM_001267550.2:c.53008C= (TTN) MANE Select	NP_001254479.2:p.Pro17670=
NM_003319.4:c.25813C= (TTN)	NP_003310.4:p.Pro8605=
NM_133378.4:c.45304C= (TTN)	NP_596869.4:p.Pro15102=
NM_133432.3:c.26188C= (TTN)	NP_597676.3:p.Pro8730=
NM_133437.4:c.26389C= (TTN)	NP_597681.4:p.Pro8797=
NR_038271.1:n.683-487G= (TTN-AS1)
XM_011511729.1:c.52105C= (TTN)	XP_011510031.1:p.Pro17369=
XM_011511730.1:c.25999C= (TTN)	XP_011510032.1:p.Pro8667=
XM_011511731.1:c.25858C= (TTN)	XP_011510033.1:p.Pro8620=
XM_017004819.1:c.51901C= (TTN)	XP_016860308.1:p.Pro17301=
XM_017004820.1:c.47299C= (TTN)	XP_016860309.1:p.Pro15767=
XM_017004821.1:c.47296C= (TTN)	XP_016860310.1:p.Pro15766=
XM_017004822.1:c.44338C= (TTN)	XP_016860311.1:p.Pro14780=
XM_017004823.1:c.25954C= (TTN)	XP_016860312.1:p.Pro8652=
XM_024453094.1:c.47449C= (TTN)	XP_024308862.1:p.Pro15817=
XM_024453095.1:c.47446C= (TTN)	XP_024308863.1:p.Pro15816=
XM_024453096.1:c.46879C= (TTN)	XP_024308864.1:p.Pro15627=
XM_024453097.1:c.44221C= (TTN)	XP_024308865.1:p.Pro14741=
XM_024453098.1:c.44140C= (TTN)	XP_024308866.1:p.Pro14714=
XM_024453099.1:c.25903C= (TTN)	XP_024308867.1:p.Pro8635=
XM_024453100.1:c.15757C= (TTN)	XP_024308868.1:p.Pro5253=