Canonical Allele Identifier: CA1310589947

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178712637_178712641delinsTACAG , CM000664.2:g.178712637_178712641delinsTACAG	GRCh38
NC_000002.11:g.179577364_179577368delinsTACAG , CM000664.1:g.179577364_179577368delinsTACAG	GRCh37
NC_000002.10:g.179285609_179285613delinsTACAG	NCBI36
NG_011618.3:g.123162_123166delinsCTGTA , LRG_391:g.123162_123166delinsCTGTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.23597-48_23597-44delinsCTGTA	ENSP00000343764.6:n.23597-48_23597-44delinsCTGTA
ENST00000342175.11:c.13858+25441_13858+25445delinsCTGTA	ENSP00000340554.6:n.13858+25441_13858+25445delinsCTGTA
ENST00000359218.10:c.13657+25441_13657+25445delinsCTGTA	ENSP00000352154.5:n.13657+25441_13657+25445delinsCTGTA
ENST00000342175.10:c.13858+25441_13858+25445delinsCTGTA	ENSP00000340554.6:n.13858+25441_13858+25445delinsCTGTA
ENST00000342992.10:c.23597-48_23597-44delinsCTGTA	ENSP00000343764.6:n.23597-48_23597-44delinsCTGTA
ENST00000359218.9:c.13657+25441_13657+25445delinsCTGTA	ENSP00000352154.5:n.13657+25441_13657+25445delinsCTGTA
ENST00000460472.6:c.13282+25441_13282+25445delinsCTGTA	ENSP00000434586.1:n.13282+25441_13282+25445delinsCTGTA
ENST00000589042.5:c.27329-48_27329-44delinsCTGTA MANE Select	ENSP00000467141.1:n.27329-48_27329-44delinsCTGTA
ENST00000591111.5:c.26378-48_26378-44delinsCTGTA	ENSP00000465570.1:n.26378-48_26378-44delinsCTGTA
ENST00000615779.4:c.26378-48_26378-44delinsCTGTA	ENSP00000483597.1:n.26378-48_26378-44delinsCTGTA
NM_001256850.1:c.26378-48_26378-44delinsCTGTA	NP_001243779.1:n.26378-48_26378-44delinsCTGTA
NM_001267550.2:c.27329-48_27329-44delinsCTGTA MANE Select	NP_001254479.2:n.27329-48_27329-44delinsCTGTA
NM_003319.4:c.13282+25441_13282+25445delinsCTGTA	NP_003310.4:n.13282+25441_13282+25445delinsCTGTA
NM_133378.4:c.23597-48_23597-44delinsCTGTA	NP_596869.4:n.23597-48_23597-44delinsCTGTA
NM_133432.3:c.13657+25441_13657+25445delinsCTGTA	NP_597676.3:n.13657+25441_13657+25445delinsCTGTA
NM_133437.4:c.13858+25441_13858+25445delinsCTGTA	NP_597681.4:n.13858+25441_13858+25445delinsCTGTA
XM_011511729.1:c.26426-48_26426-44delinsCTGTA	XP_011510031.1:n.26426-48_26426-44delinsCTGTA
XM_011511730.1:c.13468+25441_13468+25445delinsCTGTA	XP_011510032.1:n.13468+25441_13468+25445delinsCTGTA
XM_011511731.1:c.13327+25441_13327+25445delinsCTGTA	XP_011510033.1:n.13327+25441_13327+25445delinsCTGTA
XM_017004819.1:c.26381-48_26381-44delinsCTGTA	XP_016860308.1:n.26381-48_26381-44delinsCTGTA
XM_017004820.1:c.23600-48_23600-44delinsCTGTA	XP_016860309.1:n.23600-48_23600-44delinsCTGTA
XM_017004821.1:c.23597-48_23597-44delinsCTGTA	XP_016860310.1:n.23597-48_23597-44delinsCTGTA
XM_017004822.1:c.26381-48_26381-44delinsCTGTA	XP_016860311.1:n.26381-48_26381-44delinsCTGTA
XM_017004823.1:c.13423+25441_13423+25445delinsCTGTA	XP_016860312.1:n.13423+25441_13423+25445delinsCTGTA
XM_024453094.1:c.26381-48_26381-44delinsCTGTA	XP_024308862.1:n.26381-48_26381-44delinsCTGTA
XM_024453095.1:c.26381-48_26381-44delinsCTGTA	XP_024308863.1:n.26381-48_26381-44delinsCTGTA
XM_024453096.1:c.26381-48_26381-44delinsCTGTA	XP_024308864.1:n.26381-48_26381-44delinsCTGTA
XM_024453097.1:c.26381-48_26381-44delinsCTGTA	XP_024308865.1:n.26381-48_26381-44delinsCTGTA
XM_024453098.1:c.26381-48_26381-44delinsCTGTA	XP_024308866.1:n.26381-48_26381-44delinsCTGTA
XM_024453099.1:c.13423+25441_13423+25445delinsCTGTA	XP_024308867.1:n.13423+25441_13423+25445delinsCTGTA