Canonical Allele Identifier: CA2510146720

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178672515_178672516insCTTGAA , CM000664.2:g.178672515_178672516insCTTGAA	GRCh38
NC_000002.11:g.179537242_179537243insCTTGAA , CM000664.1:g.179537242_179537243insCTTGAA	GRCh37
NC_000002.10:g.179245487_179245488insCTTGAA	NCBI36
NG_011618.3:g.163287_163288insTTCAAG , LRG_391:g.163287_163288insTTCAAG

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.34856-35_34856-34insTTCAAG MANE Select	NP_001254479.2:n.34856-35_34856-34insTTCAAG
ENST00000589042.5:c.34856-35_34856-34insTTCAAG MANE Select	ENSP00000467141.1:n.34856-35_34856-34insTTCAAG
NM_001256850.1:c.33734-35_33734-34insTTCAAG	NP_001243779.1:n.33734-35_33734-34insTTCAAG
NM_003319.4:c.13283-30199_13283-30198insTTCAAG	NP_003310.4:n.13283-30199_13283-30198insTTCAAG
NM_133378.4:c.30953-35_30953-34insTTCAAG	NP_596869.4:n.30953-35_30953-34insTTCAAG
NM_133432.3:c.13658-30199_13658-30198insTTCAAG	NP_597676.3:n.13658-30199_13658-30198insTTCAAG
NM_133437.4:c.13859-30199_13859-30198insTTCAAG	NP_597681.4:n.13859-30199_13859-30198insTTCAAG
ENST00000342175.10:c.13859-30199_13859-30198insTTCAAG	ENSP00000340554.6:n.13859-30199_13859-30198insTTCAAG
ENST00000342175.11:c.13859-30199_13859-30198insTTCAAG	ENSP00000340554.6:n.13859-30199_13859-30198insTTCAAG
ENST00000342992.10:c.30953-35_30953-34insTTCAAG	ENSP00000343764.6:n.30953-35_30953-34insTTCAAG
ENST00000342992.11:c.30953-35_30953-34insTTCAAG	ENSP00000343764.6:n.30953-35_30953-34insTTCAAG
ENST00000359218.10:c.13658-30199_13658-30198insTTCAAG	ENSP00000352154.5:n.13658-30199_13658-30198insTTCAAG
ENST00000359218.9:c.13658-30199_13658-30198insTTCAAG	ENSP00000352154.5:n.13658-30199_13658-30198insTTCAAG
ENST00000414766.5:c.2440+1117_2440+1118insTTCAAG	ENSP00000401501.1:n.2440+1117_2440+1118insTTCAAG
ENST00000460472.6:c.13283-30199_13283-30198insTTCAAG	ENSP00000434586.1:n.13283-30199_13283-30198insTTCAAG
ENST00000591111.5:c.33734-35_33734-34insTTCAAG	ENSP00000465570.1:n.33734-35_33734-34insTTCAAG
ENST00000615779.4:c.33734-35_33734-34insTTCAAG	ENSP00000483597.1:n.33734-35_33734-34insTTCAAG
XM_011511729.1:c.33953-35_33953-34insTTCAAG	XP_011510031.1:n.33953-35_33953-34insTTCAAG
XM_011511730.1:c.13469-30199_13469-30198insTTCAAG	XP_011510032.1:n.13469-30199_13469-30198insTTCAAG
XM_011511731.1:c.13328-30199_13328-30198insTTCAAG	XP_011510033.1:n.13328-30199_13328-30198insTTCAAG
XM_017004819.1:c.33908-35_33908-34insTTCAAG	XP_016860308.1:n.33908-35_33908-34insTTCAAG
XM_017004820.1:c.30956-35_30956-34insTTCAAG	XP_016860309.1:n.30956-35_30956-34insTTCAAG
XM_017004821.1:c.30953-35_30953-34insTTCAAG	XP_016860310.1:n.30953-35_30953-34insTTCAAG
XM_017004822.1:c.31858+1117_31858+1118insTTCAAG	XP_016860311.1:n.31858+1117_31858+1118insTTCAAG
XM_017004823.1:c.13424-30199_13424-30198insTTCAAG	XP_016860312.1:n.13424-30199_13424-30198insTTCAAG
XM_024453094.1:c.33220+1117_33220+1118insTTCAAG	XP_024308862.1:n.33220+1117_33220+1118insTTCAAG
XM_024453095.1:c.33295+1117_33295+1118insTTCAAG	XP_024308863.1:n.33295+1117_33295+1118insTTCAAG
XM_024453096.1:c.32650+1117_32650+1118insTTCAAG	XP_024308864.1:n.32650+1117_32650+1118insTTCAAG
XM_024453097.1:c.31690+1117_31690+1118insTTCAAG	XP_024308865.1:n.31690+1117_31690+1118insTTCAAG
XM_024453098.1:c.31609+1117_31609+1118insTTCAAG	XP_024308866.1:n.31609+1117_31609+1118insTTCAAG
XM_024453099.1:c.13424-30199_13424-30198insTTCAAG	XP_024308867.1:n.13424-30199_13424-30198insTTCAAG