Canonical Allele Identifier: CA1310525757

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178557374G= , CM000664.2:g.178557374G=	GRCh38
NC_000002.11:g.179422101G= , CM000664.1:g.179422101G=	GRCh37
NC_000002.10:g.179130347G=	NCBI36
NG_011618.3:g.278429C= , LRG_391:g.278429C=
NG_051363.1:g.39548G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.80184C= (TTN)	ENSP00000343764.6:p.His26728=
ENST00000342175.11:c.61269C= (TTN)	ENSP00000340554.6:p.His20423=
ENST00000359218.10:c.61068C= (TTN)	ENSP00000352154.5:p.His20356=
ENST00000342175.10:c.61269C= (TTN)	ENSP00000340554.6:p.His20423=
ENST00000342992.10:c.80184C= (TTN)	ENSP00000343764.6:p.His26728=
ENST00000359218.9:c.61068C= (TTN)	ENSP00000352154.5:p.His20356=
ENST00000460472.6:c.60693C= (TTN)	ENSP00000434586.1:p.His20231=
ENST00000589042.5:c.87888C= (TTN) MANE Select	ENSP00000467141.1:p.His29296=
ENST00000591111.5:c.82965C= (TTN)	ENSP00000465570.1:p.His27655=
ENST00000615779.4:c.82965C= (TTN)	ENSP00000483597.1:p.His27655=
NM_001256850.1:c.82965C= (TTN)	NP_001243779.1:p.His27655=
NM_001267550.2:c.87888C= (TTN) MANE Select	NP_001254479.2:p.His29296=
NM_003319.4:c.60693C= (TTN)	NP_003310.4:p.His20231=
NM_133378.4:c.80184C= (TTN)	NP_596869.4:p.His26728=
NM_133432.3:c.61068C= (TTN)	NP_597676.3:p.His20356=
NM_133437.4:c.61269C= (TTN)	NP_597681.4:p.His20423=
NR_038271.1:n.447-13926G= (TTN-AS1)
NR_038272.1:n.2043+15013G= (TTN-AS1)
XM_011511729.1:c.86985C= (TTN)	XP_011510031.1:p.His28995=
XM_011511730.1:c.60879C= (TTN)	XP_011510032.1:p.His20293=
XM_011511731.1:c.60738C= (TTN)	XP_011510033.1:p.His20246=
XM_017004819.1:c.86781C= (TTN)	XP_016860308.1:p.His28927=
XM_017004820.1:c.82179C= (TTN)	XP_016860309.1:p.His27393=
XM_017004821.1:c.82176C= (TTN)	XP_016860310.1:p.His27392=
XM_017004822.1:c.79218C= (TTN)	XP_016860311.1:p.His26406=
XM_017004823.1:c.60834C= (TTN)	XP_016860312.1:p.His20278=
XM_024453094.1:c.82329C= (TTN)	XP_024308862.1:p.His27443=
XM_024453095.1:c.82326C= (TTN)	XP_024308863.1:p.His27442=
XM_024453096.1:c.81759C= (TTN)	XP_024308864.1:p.His27253=
XM_024453097.1:c.79101C= (TTN)	XP_024308865.1:p.His26367=
XM_024453098.1:c.79020C= (TTN)	XP_024308866.1:p.His26340=
XM_024453099.1:c.60783C= (TTN)	XP_024308867.1:p.His20261=
XM_024453100.1:c.50637C= (TTN)	XP_024308868.1:p.His16879=