Canonical Allele Identifier: CA349569837

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178607884G>A , CM000664.2:g.178607884G>A	GRCh38
NC_000002.11:g.179472611G>A , CM000664.1:g.179472611G>A	GRCh37
NC_000002.10:g.179180856G>A	NCBI36
NG_011618.3:g.227919C>T , LRG_391:g.227919C>T
NG_051363.1:g.90058G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.52903C>T (TTN) MANE Select	NP_001254479.2:p.Arg17635Ter
ENST00000589042.5:c.52903C>T (TTN) MANE Select	ENSP00000467141.1:p.Arg17635Ter
NM_001256850.1:c.47980C>T (TTN)	NP_001243779.1:p.Arg15994Ter
NM_003319.4:c.25708C>T (TTN)	NP_003310.4:p.Arg8570Ter
NM_133378.4:c.45199C>T (TTN)	NP_596869.4:p.Arg15067Ter
NM_133432.3:c.26083C>T (TTN)	NP_597676.3:p.Arg8695Ter
NM_133437.4:c.26284C>T (TTN)	NP_597681.4:p.Arg8762Ter
NR_038271.1:n.683-283G>A (TTN-AS1)
ENST00000342175.10:c.26284C>T (TTN)	ENSP00000340554.6:p.Arg8762Ter
ENST00000342175.11:c.26284C>T (TTN)	ENSP00000340554.6:p.Arg8762Ter
ENST00000342992.10:c.45199C>T (TTN)	ENSP00000343764.6:p.Arg15067Ter
ENST00000342992.11:c.45199C>T (TTN)	ENSP00000343764.6:p.Arg15067Ter
ENST00000359218.10:c.26083C>T (TTN)	ENSP00000352154.5:p.Arg8695Ter
ENST00000359218.9:c.26083C>T (TTN)	ENSP00000352154.5:p.Arg8695Ter
ENST00000460472.6:c.25708C>T (TTN)	ENSP00000434586.1:p.Arg8570Ter
ENST00000591111.5:c.47980C>T (TTN)	ENSP00000465570.1:p.Arg15994Ter
ENST00000615779.4:c.47980C>T (TTN)	ENSP00000483597.1:p.Arg15994Ter
XM_011511729.1:c.52000C>T (TTN)	XP_011510031.1:p.Arg17334Ter
XM_011511730.1:c.25894C>T (TTN)	XP_011510032.1:p.Arg8632Ter
XM_011511731.1:c.25753C>T (TTN)	XP_011510033.1:p.Arg8585Ter
XM_017004819.1:c.51796C>T (TTN)	XP_016860308.1:p.Arg17266Ter
XM_017004820.1:c.47194C>T (TTN)	XP_016860309.1:p.Arg15732Ter
XM_017004821.1:c.47191C>T (TTN)	XP_016860310.1:p.Arg15731Ter
XM_017004822.1:c.44233C>T (TTN)	XP_016860311.1:p.Arg14745Ter
XM_017004823.1:c.25849C>T (TTN)	XP_016860312.1:p.Arg8617Ter
XM_024453094.1:c.47344C>T (TTN)	XP_024308862.1:p.Arg15782Ter
XM_024453095.1:c.47341C>T (TTN)	XP_024308863.1:p.Arg15781Ter
XM_024453096.1:c.46774C>T (TTN)	XP_024308864.1:p.Arg15592Ter
XM_024453097.1:c.44116C>T (TTN)	XP_024308865.1:p.Arg14706Ter
XM_024453098.1:c.44035C>T (TTN)	XP_024308866.1:p.Arg14679Ter
XM_024453099.1:c.25798C>T (TTN)	XP_024308867.1:p.Arg8600Ter
XM_024453100.1:c.15652C>T (TTN)	XP_024308868.1:p.Arg5218Ter