Canonical Allele Identifier: CA1310534239

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178577923_178577929delinsCAAACAA , CM000664.2:g.178577923_178577929delinsCAAACAA	GRCh38
NC_000002.11:g.179442650_179442656delinsCAAACAA , CM000664.1:g.179442650_179442656delinsCAAACAA	GRCh37
NC_000002.10:g.179150896_179150902delinsCAAACAA	NCBI36
NG_011618.3:g.257874_257880delinsTTGTTTG , LRG_391:g.257874_257880delinsTTGTTTG
NG_051363.1:g.60097_60103delinsCAAACAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.60824-31_60824-25delinsTTGTTTG (TTN)	ENSP00000343764.6:n.60824-31_60824-25delinsTTGTTTG
ENST00000342175.11:c.41909-31_41909-25delinsTTGTTTG (TTN)	ENSP00000340554.6:n.41909-31_41909-25delinsTTGTTTG
ENST00000359218.10:c.41708-31_41708-25delinsTTGTTTG (TTN)	ENSP00000352154.5:n.41708-31_41708-25delinsTTGTTTG
ENST00000342175.10:c.41909-31_41909-25delinsTTGTTTG (TTN)	ENSP00000340554.6:n.41909-31_41909-25delinsTTGTTTG
ENST00000342992.10:c.60824-31_60824-25delinsTTGTTTG (TTN)	ENSP00000343764.6:n.60824-31_60824-25delinsTTGTTTG
ENST00000359218.9:c.41708-31_41708-25delinsTTGTTTG (TTN)	ENSP00000352154.5:n.41708-31_41708-25delinsTTGTTTG
ENST00000460472.6:c.41333-31_41333-25delinsTTGTTTG (TTN)	ENSP00000434586.1:n.41333-31_41333-25delinsTTGTTTG
ENST00000589042.5:c.68528-31_68528-25delinsTTGTTTG (TTN) MANE Select	ENSP00000467141.1:n.68528-31_68528-25delinsTTGTTTG
ENST00000591111.5:c.63605-31_63605-25delinsTTGTTTG (TTN)	ENSP00000465570.1:n.63605-31_63605-25delinsTTGTTTG
ENST00000615779.4:c.63605-31_63605-25delinsTTGTTTG (TTN)	ENSP00000483597.1:n.63605-31_63605-25delinsTTGTTTG
NM_001256850.1:c.63605-31_63605-25delinsTTGTTTG (TTN)	NP_001243779.1:n.63605-31_63605-25delinsTTGTTTG
NM_001267550.2:c.68528-31_68528-25delinsTTGTTTG (TTN) MANE Select	NP_001254479.2:n.68528-31_68528-25delinsTTGTTTG
NM_003319.4:c.41333-31_41333-25delinsTTGTTTG (TTN)	NP_003310.4:n.41333-31_41333-25delinsTTGTTTG
NM_133378.4:c.60824-31_60824-25delinsTTGTTTG (TTN)	NP_596869.4:n.60824-31_60824-25delinsTTGTTTG
NM_133432.3:c.41708-31_41708-25delinsTTGTTTG (TTN)	NP_597676.3:n.41708-31_41708-25delinsTTGTTTG
NM_133437.4:c.41909-31_41909-25delinsTTGTTTG (TTN)	NP_597681.4:n.41909-31_41909-25delinsTTGTTTG
NR_038271.1:n.596+6474_596+6480delinsCAAACAA (TTN-AS1)
NR_038272.1:n.2044-4649_2044-4643delinsCAAACAA (TTN-AS1)
XM_011511729.1:c.67625-31_67625-25delinsTTGTTTG (TTN)	XP_011510031.1:n.67625-31_67625-25delinsTTGTTTG
XM_011511730.1:c.41519-31_41519-25delinsTTGTTTG (TTN)	XP_011510032.1:n.41519-31_41519-25delinsTTGTTTG
XM_011511731.1:c.41378-31_41378-25delinsTTGTTTG (TTN)	XP_011510033.1:n.41378-31_41378-25delinsTTGTTTG
XM_017004819.1:c.67421-31_67421-25delinsTTGTTTG (TTN)	XP_016860308.1:n.67421-31_67421-25delinsTTGTTTG
XM_017004820.1:c.62819-31_62819-25delinsTTGTTTG (TTN)	XP_016860309.1:n.62819-31_62819-25delinsTTGTTTG
XM_017004821.1:c.62816-31_62816-25delinsTTGTTTG (TTN)	XP_016860310.1:n.62816-31_62816-25delinsTTGTTTG
XM_017004822.1:c.59858-31_59858-25delinsTTGTTTG (TTN)	XP_016860311.1:n.59858-31_59858-25delinsTTGTTTG
XM_017004823.1:c.41474-31_41474-25delinsTTGTTTG (TTN)	XP_016860312.1:n.41474-31_41474-25delinsTTGTTTG
XM_024453094.1:c.62969-31_62969-25delinsTTGTTTG (TTN)	XP_024308862.1:n.62969-31_62969-25delinsTTGTTTG
XM_024453095.1:c.62966-31_62966-25delinsTTGTTTG (TTN)	XP_024308863.1:n.62966-31_62966-25delinsTTGTTTG
XM_024453096.1:c.62399-31_62399-25delinsTTGTTTG (TTN)	XP_024308864.1:n.62399-31_62399-25delinsTTGTTTG
XM_024453097.1:c.59741-31_59741-25delinsTTGTTTG (TTN)	XP_024308865.1:n.59741-31_59741-25delinsTTGTTTG
XM_024453098.1:c.59660-31_59660-25delinsTTGTTTG (TTN)	XP_024308866.1:n.59660-31_59660-25delinsTTGTTTG
XM_024453099.1:c.41423-31_41423-25delinsTTGTTTG (TTN)	XP_024308867.1:n.41423-31_41423-25delinsTTGTTTG
XM_024453100.1:c.31277-31_31277-25delinsTTGTTTG (TTN)	XP_024308868.1:n.31277-31_31277-25delinsTTGTTTG