Canonical Allele Identifier: CA1310556157

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178630926C= , CM000664.2:g.178630926C=	GRCh38
NC_000002.11:g.179495653C= , CM000664.1:g.179495653C=	GRCh37
NC_000002.10:g.179203898C=	NCBI36
NG_011618.3:g.204877G= , LRG_391:g.204877G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.36328G=	ENSP00000343764.6:p.Val12110=
ENST00000342175.11:c.17413G=	ENSP00000340554.6:p.Val5805=
ENST00000359218.10:c.17212G=	ENSP00000352154.5:p.Val5738=
ENST00000342175.10:c.17413G=	ENSP00000340554.6:p.Val5805=
ENST00000342992.10:c.36328G=	ENSP00000343764.6:p.Val12110=
ENST00000359218.9:c.17212G=	ENSP00000352154.5:p.Val5738=
ENST00000460472.6:c.16837G=	ENSP00000434586.1:p.Val5613=
ENST00000589042.5:c.44032G= MANE Select	ENSP00000467141.1:p.Val14678=
ENST00000591111.5:c.39109G=	ENSP00000465570.1:p.Val13037=
ENST00000615779.4:c.39109G=	ENSP00000483597.1:p.Val13037=
NM_001256850.1:c.39109G=	NP_001243779.1:p.Val13037=
NM_001267550.2:c.44032G= MANE Select	NP_001254479.2:p.Val14678=
NM_003319.4:c.16837G=	NP_003310.4:p.Val5613=
NM_133378.4:c.36328G=	NP_596869.4:p.Val12110=
NM_133432.3:c.17212G=	NP_597676.3:p.Val5738=
NM_133437.4:c.17413G=	NP_597681.4:p.Val5805=
XM_011511729.1:c.43129G=	XP_011510031.1:p.Val14377=
XM_011511730.1:c.17023G=	XP_011510032.1:p.Val5675=
XM_011511731.1:c.16882G=	XP_011510033.1:p.Val5628=
XM_017004819.1:c.42925G=	XP_016860308.1:p.Val14309=
XM_017004820.1:c.38323G=	XP_016860309.1:p.Val12775=
XM_017004821.1:c.38320G=	XP_016860310.1:p.Val12774=
XM_017004822.1:c.35362G=	XP_016860311.1:p.Val11788=
XM_017004823.1:c.16978G=	XP_016860312.1:p.Val5660=
XM_024453094.1:c.38473G=	XP_024308862.1:p.Val12825=
XM_024453095.1:c.38470G=	XP_024308863.1:p.Val12824=
XM_024453096.1:c.37903G=	XP_024308864.1:p.Val12635=
XM_024453097.1:c.35245G=	XP_024308865.1:p.Val11749=
XM_024453098.1:c.35164G=	XP_024308866.1:p.Val11722=
XM_024453099.1:c.16927G=	XP_024308867.1:p.Val5643=
XM_024453100.1:c.6781G=	XP_024308868.1:p.Val2261=