Canonical Allele Identifier: CA1310589958

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178712666_178712667delinsCG , CM000664.2:g.178712666_178712667delinsCG	GRCh38
NC_000002.11:g.179577393_179577394delinsCG , CM000664.1:g.179577393_179577394delinsCG	GRCh37
NC_000002.10:g.179285638_179285639delinsCG	NCBI36
NG_011618.3:g.123136_123137delinsCG , LRG_391:g.123136_123137delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.23596+30_23596+31delinsCG	ENSP00000343764.6:n.23596+30_23596+31delinsCG
ENST00000342175.11:c.13858+25415_13858+25416delinsCG	ENSP00000340554.6:n.13858+25415_13858+25416delinsCG
ENST00000359218.10:c.13657+25415_13657+25416delinsCG	ENSP00000352154.5:n.13657+25415_13657+25416delinsCG
ENST00000342175.10:c.13858+25415_13858+25416delinsCG	ENSP00000340554.6:n.13858+25415_13858+25416delinsCG
ENST00000342992.10:c.23596+30_23596+31delinsCG	ENSP00000343764.6:n.23596+30_23596+31delinsCG
ENST00000359218.9:c.13657+25415_13657+25416delinsCG	ENSP00000352154.5:n.13657+25415_13657+25416delinsCG
ENST00000460472.6:c.13282+25415_13282+25416delinsCG	ENSP00000434586.1:n.13282+25415_13282+25416delinsCG
ENST00000589042.5:c.27328+30_27328+31delinsCG MANE Select	ENSP00000467141.1:n.27328+30_27328+31delinsCG
ENST00000591111.5:c.26377+30_26377+31delinsCG	ENSP00000465570.1:n.26377+30_26377+31delinsCG
ENST00000615779.4:c.26377+30_26377+31delinsCG	ENSP00000483597.1:n.26377+30_26377+31delinsCG
NM_001256850.1:c.26377+30_26377+31delinsCG	NP_001243779.1:n.26377+30_26377+31delinsCG
NM_001267550.2:c.27328+30_27328+31delinsCG MANE Select	NP_001254479.2:n.27328+30_27328+31delinsCG
NM_003319.4:c.13282+25415_13282+25416delinsCG	NP_003310.4:n.13282+25415_13282+25416delinsCG
NM_133378.4:c.23596+30_23596+31delinsCG	NP_596869.4:n.23596+30_23596+31delinsCG
NM_133432.3:c.13657+25415_13657+25416delinsCG	NP_597676.3:n.13657+25415_13657+25416delinsCG
NM_133437.4:c.13858+25415_13858+25416delinsCG	NP_597681.4:n.13858+25415_13858+25416delinsCG
XM_011511729.1:c.26425+30_26425+31delinsCG	XP_011510031.1:n.26425+30_26425+31delinsCG
XM_011511730.1:c.13468+25415_13468+25416delinsCG	XP_011510032.1:n.13468+25415_13468+25416delinsCG
XM_011511731.1:c.13327+25415_13327+25416delinsCG	XP_011510033.1:n.13327+25415_13327+25416delinsCG
XM_017004819.1:c.26380+30_26380+31delinsCG	XP_016860308.1:n.26380+30_26380+31delinsCG
XM_017004820.1:c.23599+30_23599+31delinsCG	XP_016860309.1:n.23599+30_23599+31delinsCG
XM_017004821.1:c.23596+30_23596+31delinsCG	XP_016860310.1:n.23596+30_23596+31delinsCG
XM_017004822.1:c.26380+30_26380+31delinsCG	XP_016860311.1:n.26380+30_26380+31delinsCG
XM_017004823.1:c.13423+25415_13423+25416delinsCG	XP_016860312.1:n.13423+25415_13423+25416delinsCG
XM_024453094.1:c.26380+30_26380+31delinsCG	XP_024308862.1:n.26380+30_26380+31delinsCG
XM_024453095.1:c.26380+30_26380+31delinsCG	XP_024308863.1:n.26380+30_26380+31delinsCG
XM_024453096.1:c.26380+30_26380+31delinsCG	XP_024308864.1:n.26380+30_26380+31delinsCG
XM_024453097.1:c.26380+30_26380+31delinsCG	XP_024308865.1:n.26380+30_26380+31delinsCG
XM_024453098.1:c.26380+30_26380+31delinsCG	XP_024308866.1:n.26380+30_26380+31delinsCG
XM_024453099.1:c.13423+25415_13423+25416delinsCG	XP_024308867.1:n.13423+25415_13423+25416delinsCG