Canonical Allele Identifier: CA1310534232

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178577916_178577931delinsAACCAGTCAAACAAAT , CM000664.2:g.178577916_178577931delinsAACCAGTCAAACAAAT	GRCh38
NC_000002.11:g.179442643_179442658delinsAACCAGTCAAACAAAT , CM000664.1:g.179442643_179442658delinsAACCAGTCAAACAAAT	GRCh37
NC_000002.10:g.179150889_179150904delinsAACCAGTCAAACAAAT	NCBI36
NG_011618.3:g.257872_257887delinsATTTGTTTGACTGGTT , LRG_391:g.257872_257887delinsATTTGTTTGACTGGTT
NG_051363.1:g.60090_60105delinsAACCAGTCAAACAAAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.60824-33_60824-18delinsATTTGTTTGACTGGTT (TTN)	ENSP00000343764.6:n.60824-33_60824-18delinsATTTGTTTGACTGGTT
ENST00000342175.11:c.41909-33_41909-18delinsATTTGTTTGACTGGTT (TTN)	ENSP00000340554.6:n.41909-33_41909-18delinsATTTGTTTGACTGGTT
ENST00000359218.10:c.41708-33_41708-18delinsATTTGTTTGACTGGTT (TTN)	ENSP00000352154.5:n.41708-33_41708-18delinsATTTGTTTGACTGGTT
ENST00000342175.10:c.41909-33_41909-18delinsATTTGTTTGACTGGTT (TTN)	ENSP00000340554.6:n.41909-33_41909-18delinsATTTGTTTGACTGGTT
ENST00000342992.10:c.60824-33_60824-18delinsATTTGTTTGACTGGTT (TTN)	ENSP00000343764.6:n.60824-33_60824-18delinsATTTGTTTGACTGGTT
ENST00000359218.9:c.41708-33_41708-18delinsATTTGTTTGACTGGTT (TTN)	ENSP00000352154.5:n.41708-33_41708-18delinsATTTGTTTGACTGGTT
ENST00000460472.6:c.41333-33_41333-18delinsATTTGTTTGACTGGTT (TTN)	ENSP00000434586.1:n.41333-33_41333-18delinsATTTGTTTGACTGGTT
ENST00000589042.5:c.68528-33_68528-18delinsATTTGTTTGACTGGTT (TTN) MANE Select	ENSP00000467141.1:n.68528-33_68528-18delinsATTTGTTTGACTGGTT
ENST00000591111.5:c.63605-33_63605-18delinsATTTGTTTGACTGGTT (TTN)	ENSP00000465570.1:n.63605-33_63605-18delinsATTTGTTTGACTGGTT
ENST00000615779.4:c.63605-33_63605-18delinsATTTGTTTGACTGGTT (TTN)	ENSP00000483597.1:n.63605-33_63605-18delinsATTTGTTTGACTGGTT
NM_001256850.1:c.63605-33_63605-18delinsATTTGTTTGACTGGTT (TTN)	NP_001243779.1:n.63605-33_63605-18delinsATTTGTTTGACTGGTT
NM_001267550.2:c.68528-33_68528-18delinsATTTGTTTGACTGGTT (TTN) MANE Select	NP_001254479.2:n.68528-33_68528-18delinsATTTGTTTGACTGGTT
NM_003319.4:c.41333-33_41333-18delinsATTTGTTTGACTGGTT (TTN)	NP_003310.4:n.41333-33_41333-18delinsATTTGTTTGACTGGTT
NM_133378.4:c.60824-33_60824-18delinsATTTGTTTGACTGGTT (TTN)	NP_596869.4:n.60824-33_60824-18delinsATTTGTTTGACTGGTT
NM_133432.3:c.41708-33_41708-18delinsATTTGTTTGACTGGTT (TTN)	NP_597676.3:n.41708-33_41708-18delinsATTTGTTTGACTGGTT
NM_133437.4:c.41909-33_41909-18delinsATTTGTTTGACTGGTT (TTN)	NP_597681.4:n.41909-33_41909-18delinsATTTGTTTGACTGGTT
NR_038271.1:n.596+6467_596+6482delinsAACCAGTCAAACAAAT (TTN-AS1)
NR_038272.1:n.2044-4656_2044-4641delinsAACCAGTCAAACAAAT (TTN-AS1)
XM_011511729.1:c.67625-33_67625-18delinsATTTGTTTGACTGGTT (TTN)	XP_011510031.1:n.67625-33_67625-18delinsATTTGTTTGACTGGTT
XM_011511730.1:c.41519-33_41519-18delinsATTTGTTTGACTGGTT (TTN)	XP_011510032.1:n.41519-33_41519-18delinsATTTGTTTGACTGGTT
XM_011511731.1:c.41378-33_41378-18delinsATTTGTTTGACTGGTT (TTN)	XP_011510033.1:n.41378-33_41378-18delinsATTTGTTTGACTGGTT
XM_017004819.1:c.67421-33_67421-18delinsATTTGTTTGACTGGTT (TTN)	XP_016860308.1:n.67421-33_67421-18delinsATTTGTTTGACTGGTT
XM_017004820.1:c.62819-33_62819-18delinsATTTGTTTGACTGGTT (TTN)	XP_016860309.1:n.62819-33_62819-18delinsATTTGTTTGACTGGTT
XM_017004821.1:c.62816-33_62816-18delinsATTTGTTTGACTGGTT (TTN)	XP_016860310.1:n.62816-33_62816-18delinsATTTGTTTGACTGGTT
XM_017004822.1:c.59858-33_59858-18delinsATTTGTTTGACTGGTT (TTN)	XP_016860311.1:n.59858-33_59858-18delinsATTTGTTTGACTGGTT
XM_017004823.1:c.41474-33_41474-18delinsATTTGTTTGACTGGTT (TTN)	XP_016860312.1:n.41474-33_41474-18delinsATTTGTTTGACTGGTT
XM_024453094.1:c.62969-33_62969-18delinsATTTGTTTGACTGGTT (TTN)	XP_024308862.1:n.62969-33_62969-18delinsATTTGTTTGACTGGTT
XM_024453095.1:c.62966-33_62966-18delinsATTTGTTTGACTGGTT (TTN)	XP_024308863.1:n.62966-33_62966-18delinsATTTGTTTGACTGGTT
XM_024453096.1:c.62399-33_62399-18delinsATTTGTTTGACTGGTT (TTN)	XP_024308864.1:n.62399-33_62399-18delinsATTTGTTTGACTGGTT
XM_024453097.1:c.59741-33_59741-18delinsATTTGTTTGACTGGTT (TTN)	XP_024308865.1:n.59741-33_59741-18delinsATTTGTTTGACTGGTT
XM_024453098.1:c.59660-33_59660-18delinsATTTGTTTGACTGGTT (TTN)	XP_024308866.1:n.59660-33_59660-18delinsATTTGTTTGACTGGTT
XM_024453099.1:c.41423-33_41423-18delinsATTTGTTTGACTGGTT (TTN)	XP_024308867.1:n.41423-33_41423-18delinsATTTGTTTGACTGGTT
XM_024453100.1:c.31277-33_31277-18delinsATTTGTTTGACTGGTT (TTN)	XP_024308868.1:n.31277-33_31277-18delinsATTTGTTTGACTGGTT