Canonical Allele Identifier: CA2838662404

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178592704_178592705insAGAATT , CM000664.2:g.178592704_178592705insAGAATT	GRCh38
NC_000002.11:g.179457431_179457432insAGAATT , CM000664.1:g.179457431_179457432insAGAATT	GRCh37
NC_000002.10:g.179165677_179165678insAGAATT	NCBI36
NG_011618.3:g.243098_243099insAATTCT , LRG_391:g.243098_243099insAATTCT
NG_051363.1:g.74878_74879insAGAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.51641-45_51641-44insAATTCT (TTN)	ENSP00000343764.6:n.51641-45_51641-44insAATTCT
ENST00000342175.11:c.32726-45_32726-44insAATTCT (TTN)	ENSP00000340554.6:n.32726-45_32726-44insAATTCT
ENST00000359218.10:c.32525-45_32525-44insAATTCT (TTN)	ENSP00000352154.5:n.32525-45_32525-44insAATTCT
ENST00000342175.10:c.32726-45_32726-44insAATTCT (TTN)	ENSP00000340554.6:n.32726-45_32726-44insAATTCT
ENST00000342992.10:c.51641-45_51641-44insAATTCT (TTN)	ENSP00000343764.6:n.51641-45_51641-44insAATTCT
ENST00000359218.9:c.32525-45_32525-44insAATTCT (TTN)	ENSP00000352154.5:n.32525-45_32525-44insAATTCT
ENST00000460472.6:c.32150-45_32150-44insAATTCT (TTN)	ENSP00000434586.1:n.32150-45_32150-44insAATTCT
ENST00000589042.5:c.59345-45_59345-44insAATTCT (TTN) MANE Select	ENSP00000467141.1:n.59345-45_59345-44insAATTCT
ENST00000591111.5:c.54422-45_54422-44insAATTCT (TTN)	ENSP00000465570.1:n.54422-45_54422-44insAATTCT
ENST00000615779.4:c.54422-45_54422-44insAATTCT (TTN)	ENSP00000483597.1:n.54422-45_54422-44insAATTCT
NM_001256850.1:c.54422-45_54422-44insAATTCT (TTN)	NP_001243779.1:n.54422-45_54422-44insAATTCT
NM_001267550.2:c.59345-45_59345-44insAATTCT (TTN) MANE Select	NP_001254479.2:n.59345-45_59345-44insAATTCT
NM_003319.4:c.32150-45_32150-44insAATTCT (TTN)	NP_003310.4:n.32150-45_32150-44insAATTCT
NM_133378.4:c.51641-45_51641-44insAATTCT (TTN)	NP_596869.4:n.51641-45_51641-44insAATTCT
NM_133432.3:c.32525-45_32525-44insAATTCT (TTN)	NP_597676.3:n.32525-45_32525-44insAATTCT
NM_133437.4:c.32726-45_32726-44insAATTCT (TTN)	NP_597681.4:n.32726-45_32726-44insAATTCT
NR_038271.1:n.597-4892_597-4891insAGAATT (TTN-AS1)
NR_038272.1:n.3364+1390_3364+1391insAGAATT (TTN-AS1)
XM_011511729.1:c.58442-45_58442-44insAATTCT (TTN)	XP_011510031.1:n.58442-45_58442-44insAATTCT
XM_011511730.1:c.32336-45_32336-44insAATTCT (TTN)	XP_011510032.1:n.32336-45_32336-44insAATTCT
XM_011511731.1:c.32195-45_32195-44insAATTCT (TTN)	XP_011510033.1:n.32195-45_32195-44insAATTCT
XM_017004819.1:c.58238-45_58238-44insAATTCT (TTN)	XP_016860308.1:n.58238-45_58238-44insAATTCT
XM_017004820.1:c.53636-45_53636-44insAATTCT (TTN)	XP_016860309.1:n.53636-45_53636-44insAATTCT
XM_017004821.1:c.53633-45_53633-44insAATTCT (TTN)	XP_016860310.1:n.53633-45_53633-44insAATTCT
XM_017004822.1:c.50675-45_50675-44insAATTCT (TTN)	XP_016860311.1:n.50675-45_50675-44insAATTCT
XM_017004823.1:c.32291-45_32291-44insAATTCT (TTN)	XP_016860312.1:n.32291-45_32291-44insAATTCT
XM_024453094.1:c.53786-45_53786-44insAATTCT (TTN)	XP_024308862.1:n.53786-45_53786-44insAATTCT
XM_024453095.1:c.53783-45_53783-44insAATTCT (TTN)	XP_024308863.1:n.53783-45_53783-44insAATTCT
XM_024453096.1:c.53216-45_53216-44insAATTCT (TTN)	XP_024308864.1:n.53216-45_53216-44insAATTCT
XM_024453097.1:c.50558-45_50558-44insAATTCT (TTN)	XP_024308865.1:n.50558-45_50558-44insAATTCT
XM_024453098.1:c.50477-45_50477-44insAATTCT (TTN)	XP_024308866.1:n.50477-45_50477-44insAATTCT
XM_024453099.1:c.32240-45_32240-44insAATTCT (TTN)	XP_024308867.1:n.32240-45_32240-44insAATTCT
XM_024453100.1:c.22094-45_22094-44insAATTCT (TTN)	XP_024308868.1:n.22094-45_22094-44insAATTCT