Canonical Allele Identifier: CA1310589277

Gene: TTN

Linked Data

• dbSNP Id: rs2076582082
• gnomAD v4: 2-178711047-T-TAATTCTAGAAATGA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178711049_178711050insTTCTAGAAATGAAA , CM000664.2:g.178711049_178711050insTTCTAGAAATGAAA	GRCh38
NC_000002.11:g.179575776_179575777insTTCTAGAAATGAAA , CM000664.1:g.179575776_179575777insTTCTAGAAATGAAA	GRCh37
NC_000002.10:g.179284021_179284022insTTCTAGAAATGAAA	NCBI36
NG_011618.3:g.124755_124756insTCATTTCTAGAATT , LRG_391:g.124755_124756insTCATTTCTAGAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.24442+14_24442+15insTCATTTCTAGAATT	ENSP00000343764.6:n.24442+14_24442+15insTCATTTCTAGAATT
ENST00000342175.11:c.13858+27034_13858+27035insTCATTTCTAGAATT	ENSP00000340554.6:n.13858+27034_13858+27035insTCATTTCTAGAATT
ENST00000359218.10:c.13657+27034_13657+27035insTCATTTCTAGAATT	ENSP00000352154.5:n.13657+27034_13657+27035insTCATTTCTAGAATT
ENST00000342175.10:c.13858+27034_13858+27035insTCATTTCTAGAATT	ENSP00000340554.6:n.13858+27034_13858+27035insTCATTTCTAGAATT
ENST00000342992.10:c.24442+14_24442+15insTCATTTCTAGAATT	ENSP00000343764.6:n.24442+14_24442+15insTCATTTCTAGAATT
ENST00000359218.9:c.13657+27034_13657+27035insTCATTTCTAGAATT	ENSP00000352154.5:n.13657+27034_13657+27035insTCATTTCTAGAATT
ENST00000460472.6:c.13282+27034_13282+27035insTCATTTCTAGAATT	ENSP00000434586.1:n.13282+27034_13282+27035insTCATTTCTAGAATT
ENST00000589042.5:c.28174+14_28174+15insTCATTTCTAGAATT MANE Select	ENSP00000467141.1:n.28174+14_28174+15insTCATTTCTAGAATT
ENST00000591111.5:c.27223+14_27223+15insTCATTTCTAGAATT	ENSP00000465570.1:n.27223+14_27223+15insTCATTTCTAGAATT
ENST00000615779.4:c.27223+14_27223+15insTCATTTCTAGAATT	ENSP00000483597.1:n.27223+14_27223+15insTCATTTCTAGAATT
NM_001256850.1:c.27223+14_27223+15insTCATTTCTAGAATT	NP_001243779.1:n.27223+14_27223+15insTCATTTCTAGAATT
NM_001267550.2:c.28174+14_28174+15insTCATTTCTAGAATT MANE Select	NP_001254479.2:n.28174+14_28174+15insTCATTTCTAGAATT
NM_003319.4:c.13282+27034_13282+27035insTCATTTCTAGAATT	NP_003310.4:n.13282+27034_13282+27035insTCATTTCTAGAATT
NM_133378.4:c.24442+14_24442+15insTCATTTCTAGAATT	NP_596869.4:n.24442+14_24442+15insTCATTTCTAGAATT
NM_133432.3:c.13657+27034_13657+27035insTCATTTCTAGAATT	NP_597676.3:n.13657+27034_13657+27035insTCATTTCTAGAATT
NM_133437.4:c.13858+27034_13858+27035insTCATTTCTAGAATT	NP_597681.4:n.13858+27034_13858+27035insTCATTTCTAGAATT
XM_011511729.1:c.27271+14_27271+15insTCATTTCTAGAATT	XP_011510031.1:n.27271+14_27271+15insTCATTTCTAGAATT
XM_011511730.1:c.13468+27034_13468+27035insTCATTTCTAGAATT	XP_011510032.1:n.13468+27034_13468+27035insTCATTTCTAGAATT
XM_011511731.1:c.13327+27034_13327+27035insTCATTTCTAGAATT	XP_011510033.1:n.13327+27034_13327+27035insTCATTTCTAGAATT
XM_017004819.1:c.27226+14_27226+15insTCATTTCTAGAATT	XP_016860308.1:n.27226+14_27226+15insTCATTTCTAGAATT
XM_017004820.1:c.24445+14_24445+15insTCATTTCTAGAATT	XP_016860309.1:n.24445+14_24445+15insTCATTTCTAGAATT
XM_017004821.1:c.24442+14_24442+15insTCATTTCTAGAATT	XP_016860310.1:n.24442+14_24442+15insTCATTTCTAGAATT
XM_017004822.1:c.27226+14_27226+15insTCATTTCTAGAATT	XP_016860311.1:n.27226+14_27226+15insTCATTTCTAGAATT
XM_017004823.1:c.13423+27034_13423+27035insTCATTTCTAGAATT	XP_016860312.1:n.13423+27034_13423+27035insTCATTTCTAGAATT
XM_024453094.1:c.27226+14_27226+15insTCATTTCTAGAATT	XP_024308862.1:n.27226+14_27226+15insTCATTTCTAGAATT
XM_024453095.1:c.27226+14_27226+15insTCATTTCTAGAATT	XP_024308863.1:n.27226+14_27226+15insTCATTTCTAGAATT
XM_024453096.1:c.27226+14_27226+15insTCATTTCTAGAATT	XP_024308864.1:n.27226+14_27226+15insTCATTTCTAGAATT
XM_024453097.1:c.27226+14_27226+15insTCATTTCTAGAATT	XP_024308865.1:n.27226+14_27226+15insTCATTTCTAGAATT
XM_024453098.1:c.27226+14_27226+15insTCATTTCTAGAATT	XP_024308866.1:n.27226+14_27226+15insTCATTTCTAGAATT
XM_024453099.1:c.13423+27034_13423+27035insTCATTTCTAGAATT	XP_024308867.1:n.13423+27034_13423+27035insTCATTTCTAGAATT