Canonical Allele Identifier: CA1310550960

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618207C= , CM000664.2:g.178618207C=	GRCh38
NC_000002.11:g.179482934C= , CM000664.1:g.179482934C=	GRCh37
NC_000002.10:g.179191179C=	NCBI36
NG_011618.3:g.217596G= , LRG_391:g.217596G=
NG_051363.1:g.100381C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.39547G= (TTN)	ENSP00000343764.6:p.Glu13183=
ENST00000342175.11:c.20632G= (TTN)	ENSP00000340554.6:p.Glu6878=
ENST00000359218.10:c.20431G= (TTN)	ENSP00000352154.5:p.Glu6811=
ENST00000342175.10:c.20632G= (TTN)	ENSP00000340554.6:p.Glu6878=
ENST00000342992.10:c.39547G= (TTN)	ENSP00000343764.6:p.Glu13183=
ENST00000359218.9:c.20431G= (TTN)	ENSP00000352154.5:p.Glu6811=
ENST00000460472.6:c.20056G= (TTN)	ENSP00000434586.1:p.Glu6686=
ENST00000589042.5:c.47251G= (TTN) MANE Select	ENSP00000467141.1:p.Glu15751=
ENST00000591111.5:c.42328G= (TTN)	ENSP00000465570.1:p.Glu14110=
ENST00000615779.4:c.42328G= (TTN)	ENSP00000483597.1:p.Glu14110=
NM_001256850.1:c.42328G= (TTN)	NP_001243779.1:p.Glu14110=
NM_001267550.2:c.47251G= (TTN) MANE Select	NP_001254479.2:p.Glu15751=
NM_003319.4:c.20056G= (TTN)	NP_003310.4:p.Glu6686=
NM_133378.4:c.39547G= (TTN)	NP_596869.4:p.Glu13183=
NM_133432.3:c.20431G= (TTN)	NP_597676.3:p.Glu6811=
NM_133437.4:c.20632G= (TTN)	NP_597681.4:p.Glu6878=
NR_038271.1:n.1605-1546C= (TTN-AS1)
XM_011511729.1:c.46348G= (TTN)	XP_011510031.1:p.Glu15450=
XM_011511730.1:c.20242G= (TTN)	XP_011510032.1:p.Glu6748=
XM_011511731.1:c.20101G= (TTN)	XP_011510033.1:p.Glu6701=
XM_017004819.1:c.46144G= (TTN)	XP_016860308.1:p.Glu15382=
XM_017004820.1:c.41542G= (TTN)	XP_016860309.1:p.Glu13848=
XM_017004821.1:c.41539G= (TTN)	XP_016860310.1:p.Glu13847=
XM_017004822.1:c.38581G= (TTN)	XP_016860311.1:p.Glu12861=
XM_017004823.1:c.20197G= (TTN)	XP_016860312.1:p.Glu6733=
XM_024453094.1:c.41692G= (TTN)	XP_024308862.1:p.Glu13898=
XM_024453095.1:c.41689G= (TTN)	XP_024308863.1:p.Glu13897=
XM_024453096.1:c.41122G= (TTN)	XP_024308864.1:p.Glu13708=
XM_024453097.1:c.38464G= (TTN)	XP_024308865.1:p.Glu12822=
XM_024453098.1:c.38383G= (TTN)	XP_024308866.1:p.Glu12795=
XM_024453099.1:c.20146G= (TTN)	XP_024308867.1:p.Glu6716=
XM_024453100.1:c.10000G= (TTN)	XP_024308868.1:p.Glu3334=