Canonical Allele Identifier: CA1310534218

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178577905_178577907delinsCAT , CM000664.2:g.178577905_178577907delinsCAT	GRCh38
NC_000002.11:g.179442632_179442634delinsCAT , CM000664.1:g.179442632_179442634delinsCAT	GRCh37
NC_000002.10:g.179150878_179150880delinsCAT	NCBI36
NG_011618.3:g.257896_257898delinsATG , LRG_391:g.257896_257898delinsATG
NG_051363.1:g.60079_60081delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.60824-9_60824-7delinsATG (TTN)	ENSP00000343764.6:n.60824-9_60824-7delinsATG
ENST00000342175.11:c.41909-9_41909-7delinsATG (TTN)	ENSP00000340554.6:n.41909-9_41909-7delinsATG
ENST00000359218.10:c.41708-9_41708-7delinsATG (TTN)	ENSP00000352154.5:n.41708-9_41708-7delinsATG
ENST00000342175.10:c.41909-9_41909-7delinsATG (TTN)	ENSP00000340554.6:n.41909-9_41909-7delinsATG
ENST00000342992.10:c.60824-9_60824-7delinsATG (TTN)	ENSP00000343764.6:n.60824-9_60824-7delinsATG
ENST00000359218.9:c.41708-9_41708-7delinsATG (TTN)	ENSP00000352154.5:n.41708-9_41708-7delinsATG
ENST00000460472.6:c.41333-9_41333-7delinsATG (TTN)	ENSP00000434586.1:n.41333-9_41333-7delinsATG
ENST00000589042.5:c.68528-9_68528-7delinsATG (TTN) MANE Select	ENSP00000467141.1:n.68528-9_68528-7delinsATG
ENST00000591111.5:c.63605-9_63605-7delinsATG (TTN)	ENSP00000465570.1:n.63605-9_63605-7delinsATG
ENST00000615779.4:c.63605-9_63605-7delinsATG (TTN)	ENSP00000483597.1:n.63605-9_63605-7delinsATG
NM_001256850.1:c.63605-9_63605-7delinsATG (TTN)	NP_001243779.1:n.63605-9_63605-7delinsATG
NM_001267550.2:c.68528-9_68528-7delinsATG (TTN) MANE Select	NP_001254479.2:n.68528-9_68528-7delinsATG
NM_003319.4:c.41333-9_41333-7delinsATG (TTN)	NP_003310.4:n.41333-9_41333-7delinsATG
NM_133378.4:c.60824-9_60824-7delinsATG (TTN)	NP_596869.4:n.60824-9_60824-7delinsATG
NM_133432.3:c.41708-9_41708-7delinsATG (TTN)	NP_597676.3:n.41708-9_41708-7delinsATG
NM_133437.4:c.41909-9_41909-7delinsATG (TTN)	NP_597681.4:n.41909-9_41909-7delinsATG
NR_038271.1:n.596+6456_596+6458delinsCAT (TTN-AS1)
NR_038272.1:n.2044-4667_2044-4665delinsCAT (TTN-AS1)
XM_011511729.1:c.67625-9_67625-7delinsATG (TTN)	XP_011510031.1:n.67625-9_67625-7delinsATG
XM_011511730.1:c.41519-9_41519-7delinsATG (TTN)	XP_011510032.1:n.41519-9_41519-7delinsATG
XM_011511731.1:c.41378-9_41378-7delinsATG (TTN)	XP_011510033.1:n.41378-9_41378-7delinsATG
XM_017004819.1:c.67421-9_67421-7delinsATG (TTN)	XP_016860308.1:n.67421-9_67421-7delinsATG
XM_017004820.1:c.62819-9_62819-7delinsATG (TTN)	XP_016860309.1:n.62819-9_62819-7delinsATG
XM_017004821.1:c.62816-9_62816-7delinsATG (TTN)	XP_016860310.1:n.62816-9_62816-7delinsATG
XM_017004822.1:c.59858-9_59858-7delinsATG (TTN)	XP_016860311.1:n.59858-9_59858-7delinsATG
XM_017004823.1:c.41474-9_41474-7delinsATG (TTN)	XP_016860312.1:n.41474-9_41474-7delinsATG
XM_024453094.1:c.62969-9_62969-7delinsATG (TTN)	XP_024308862.1:n.62969-9_62969-7delinsATG
XM_024453095.1:c.62966-9_62966-7delinsATG (TTN)	XP_024308863.1:n.62966-9_62966-7delinsATG
XM_024453096.1:c.62399-9_62399-7delinsATG (TTN)	XP_024308864.1:n.62399-9_62399-7delinsATG
XM_024453097.1:c.59741-9_59741-7delinsATG (TTN)	XP_024308865.1:n.59741-9_59741-7delinsATG
XM_024453098.1:c.59660-9_59660-7delinsATG (TTN)	XP_024308866.1:n.59660-9_59660-7delinsATG
XM_024453099.1:c.41423-9_41423-7delinsATG (TTN)	XP_024308867.1:n.41423-9_41423-7delinsATG
XM_024453100.1:c.31277-9_31277-7delinsATG (TTN)	XP_024308868.1:n.31277-9_31277-7delinsATG